alcohols, phenols & ethers - karnataka...
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![Page 1: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/1.jpg)
Alcohols, Phenols & Ethers
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![Page 2: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/2.jpg)
1. Alcohols boil at higher temperature thanthe corresponding hydrocarbons due to
(A) intermolecular hydrogen bonding(B) intramolecular hydrogen bonding(C) van der Waal’s forces of attraction(D) dipole – dipole interactions
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1. Alcohols boil at higher temperature thanthe corresponding hydrocarbons due to
(A) intermolecular hydrogen bonding(B) intramolecular hydrogen bonding(C) van der Waal’s forces of attraction(D) dipole – dipole interactions
![Page 3: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/3.jpg)
Ans: (A)
Ans: (A)
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![Page 4: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/4.jpg)
2. Vinyl carbinol is ____________
(A)(B)(C)(D)
2 2CH CH CH OH
3CH CH CH OH
3CH CH CH OH
3 2CH C(OH) CH
2CH CH OH
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2. Vinyl carbinol is ____________
(A)(B)(C)(D) 3CH CH CH OH
![Page 5: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/5.jpg)
Carbinol is CH3OH, which is attached tovinyl group. Therefore Ans is (C)
2CH CH OH
2 2CH CH CH OH
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2 2CH CH CH OH
![Page 6: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/6.jpg)
3. 1-propanol and 2-propanol can be bestdistinguished by(A) Oxidation with alk. KMnO4 followed by
reaction with Fehling solution(B) Oxidation with acidic dichromate followed
by reaction with Fehling solution(C) Oxidation by heating with copper followed
by reaction with Fehling solution.(D) Oxidation with conc. H2SO4 followed by
reaction with Fehling solution.
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3. 1-propanol and 2-propanol can be bestdistinguished by(A) Oxidation with alk. KMnO4 followed by
reaction with Fehling solution(B) Oxidation with acidic dichromate followed
by reaction with Fehling solution(C) Oxidation by heating with copper followed
by reaction with Fehling solution.(D) Oxidation with conc. H2SO4 followed by
reaction with Fehling solution.
![Page 7: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/7.jpg)
red colour.No reaction.
Ans (C)
Cu Fehling3 2 2 3 2 Soln
CH CH CH OH CH CH CHO s
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red colour.No reaction.
Ans (C)
Cu Fehling3 3 3 3 Soln
CH CH CH CH COCH|OH
![Page 8: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/8.jpg)
4. Phenyl magnesium bromide reacts withmethanol to give
(A) a mixture of anisols and Mg(OH)Br(B) a mixture of benzene and Mg(OMe)Br(C) a mixture of toluene and Mg (OH)Br(D) a mixture of phenol and Mg(OH)Br
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4. Phenyl magnesium bromide reacts withmethanol to give
(A) a mixture of anisols and Mg(OH)Br(B) a mixture of benzene and Mg(OMe)Br(C) a mixture of toluene and Mg (OH)Br(D) a mixture of phenol and Mg(OH)Br
![Page 9: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/9.jpg)
Ans: (B)
6 5 3 6 6C H MgBr CH OH C H Mg(OMe)Br
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Ans: (B)
![Page 10: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/10.jpg)
5) Reduction of aldehyde, RCHO withsodium and ethanol gives
(A) 1° alcohol
(B) 2° alcohol
(C) 3° alcohol
(D) alkane
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5) Reduction of aldehyde, RCHO withsodium and ethanol gives
(A) 1° alcohol
(B) 2° alcohol
(C) 3° alcohol
(D) alkane
![Page 11: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/11.jpg)
Ans: A) 1° alcohol
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Ans: A) 1° alcohol
![Page 12: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/12.jpg)
6) Which of the following compound willproduce a primary alcohol on reaction withGrignard reagent followed by hydrolysis?
(A) acetone (B)methyl cyanide
(C) ethylene oxide (D) ethyl acetate
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6) Which of the following compound willproduce a primary alcohol on reaction withGrignard reagent followed by hydrolysis?
(A) acetone (B)methyl cyanide
(C) ethylene oxide (D) ethyl acetate
![Page 13: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/13.jpg)
Grignard reagent is converted into 1° alcoholusing H−CHO or ethyleneoxide
1° alcohol containing 2 carbon atoms more thanthe Grignard reagent can be obtained by treatingwith R-Mg-X with ethylene oxide followed byacid hydrolysis,
Ans: (C) ethylene oxide
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Grignard reagent is converted into 1° alcoholusing H−CHO or ethyleneoxide
1° alcohol containing 2 carbon atoms more thanthe Grignard reagent can be obtained by treatingwith R-Mg-X with ethylene oxide followed byacid hydrolysis,
Ans: (C) ethylene oxide
![Page 14: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/14.jpg)
7) The compound X in the reaction is
(A) (B)
(C) (CH3)2CH(OMgBr) (D)
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7) The compound X in the reaction is
(A) (B)
(C) (CH3)2CH(OMgBr) (D)
![Page 15: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/15.jpg)
Ans:
(C) (CH3)2CH(OMgBr)
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Ans:
(C) (CH3)2CH(OMgBr)
![Page 16: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/16.jpg)
8. In the following sequence of reaction:The compound D is
(A) 2-propanal (B) 1-propanal(C) 1-butanol (D) 2-butanal
2 2P I H OMg HCHO3 2 2 ether
CH CH CH OH A B C D
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8. In the following sequence of reaction:The compound D is
(A) 2-propanal (B) 1-propanal(C) 1-butanol (D) 2-butanal
![Page 17: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/17.jpg)
2P/I Mg3 2 2 3 2 2 3 2 3ether
HCHO3 2 2 2
CH CH CH OH CH CH CH I CH CH CH MgI
CH CH CH CH OMgI
1-butanol +Mg(OH)I
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2P/I Mg3 2 2 3 2 2 3 2 3ether
HCHO3 2 2 2
CH CH CH OH CH CH CH I CH CH CH MgI
CH CH CH CH OMgI
1-butanol +Mg(OH)IH2O
Ans: (C)
![Page 18: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/18.jpg)
9. Which one of the following is most acidic?
(A)CH3OH(B)CH3CH2OH(C) (CH3)2CHOH(D) (CH3)3COH
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9. Which one of the following is most acidic?
(A)CH3OH(B)CH3CH2OH(C) (CH3)2CHOH(D) (CH3)3COH
![Page 19: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/19.jpg)
Due to the electron releasing groups in othercompounds.Ans: (a) CH3OH
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![Page 20: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/20.jpg)
10. Which one of the following is most acidic?
(A)H2O (B) CH3CH2OH(C) CH3OCH3 (D) C6H5OH
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10. Which one of the following is most acidic?
(A)H2O (B) CH3CH2OH(C) CH3OCH3 (D) C6H5OH
![Page 21: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/21.jpg)
C6H5OHDue the presence of more electro negativeSp2 hybridised carbon of benzene.
Ans: (D)
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C6H5OHDue the presence of more electro negativeSp2 hybridised carbon of benzene.
Ans: (D)
![Page 22: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/22.jpg)
11)The reactivity of alcohol towardsactive metal is
(A) 3° > 2° > 1°
(B) 1° > 2° > 3°
(C) 3° > 1° > 2°
(D) 2° < 3° < 1°22
11)The reactivity of alcohol towardsactive metal is
(A) 3° > 2° > 1°
(B) 1° > 2° > 3°
(C) 3° > 1° > 2°
(D) 2° < 3° < 1°
![Page 23: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/23.jpg)
When an alcohol reacts with a metal, forexample, sodium, bond between RO−H isbroken for which 1° alcohols are mostreactive since 1° alcohols are more acidicthan 3° alcohols which is least reactive.
Ans (B) 1° > 2° > 3°
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When an alcohol reacts with a metal, forexample, sodium, bond between RO−H isbroken for which 1° alcohols are mostreactive since 1° alcohols are more acidicthan 3° alcohols which is least reactive.
Ans (B) 1° > 2° > 3°
![Page 24: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/24.jpg)
12) Pentan-3-ol is an example of –
(A)1 alcohol(B) 2 alcohol(C) 3 alcohol(D) aromatic alcohol
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12) Pentan-3-ol is an example of –
(A)1 alcohol(B) 2 alcohol(C) 3 alcohol(D) aromatic alcohol
![Page 25: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/25.jpg)
Ans: (B)
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![Page 26: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/26.jpg)
13. How many optically active isomers arepossible for butane-2, 3-diol?
(A) 1 (B) 2 (C) 3 (D) 4
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![Page 27: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/27.jpg)
Ans: (B) There are 2 chiral carbons but due tothe presence of symmetry, the compoundshows two optically active isomers only
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Ans: (B) There are 2 chiral carbons but due tothe presence of symmetry, the compoundshows two optically active isomers only
H C OH
H C OH
CH3
CH3
H C OH
HO C H
CH3
CH3
![Page 28: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/28.jpg)
14) The order of reactivity of a Grignardreagent with the following is
I) CH3-CO-CH3
II) CH3-CHOIII) C6H5-CO-C6H5
(A) II > III > I (B) I > III > II(C) II > I > III (D) all react with same rate
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14) The order of reactivity of a Grignardreagent with the following is
I) CH3-CO-CH3
II) CH3-CHOIII) C6H5-CO-C6H5
(A) II > III > I (B) I > III > II(C) II > I > III (D) all react with same rate
![Page 29: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/29.jpg)
Reactivity is high when steric hindranceis the least.
C) II > I > III
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Reactivity is high when steric hindranceis the least.
C) II > I > III
![Page 30: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/30.jpg)
15. 0.037 g of an alcohol was added to CH3MgIand the gas evolved measured 11.2 cm3 atSTP. What is the molecular formula of thealcohol?
(A)C4H10O (B) C4H8O(C) C5H12O (D) C5H10O
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15. 0.037 g of an alcohol was added to CH3MgIand the gas evolved measured 11.2 cm3 atSTP. What is the molecular formula of thealcohol?
(A)C4H10O (B) C4H8O(C) C5H12O (D) C5H10O
![Page 31: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/31.jpg)
311.2 cm 0.037 g of alc
0.037 2240074 g
11.2
• C4H10O
• 22400 cm3 of the gas liberated by
alc
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0.037 2240074 g
11.2
• C4H10O
Ans: (A)
![Page 32: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/32.jpg)
16. In the following sequence of reaction.
The compound A is
(A)CH3CH2CH2CH2OH(B) (CH3)2CHOH(C) (CH3)3COH(D) CH3CH2COCH2CH3
Cu HBr aq.KOH3 3573
A B C (CH ) COH
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16. In the following sequence of reaction.
The compound A is
(A)CH3CH2CH2CH2OH(B) (CH3)2CHOH(C) (CH3)3COH(D) CH3CH2COCH2CH3
![Page 33: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/33.jpg)
Tertiary alcohols undergo dehydration togive an alkene ,2-methyl propene which onreaction with HBr gives addition productaccording to Mark Rule. That on KOHtreatment gives tertiary butyl alcoholAns: (C)
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Tertiary alcohols undergo dehydration togive an alkene ,2-methyl propene which onreaction with HBr gives addition productaccording to Mark Rule. That on KOHtreatment gives tertiary butyl alcoholAns: (C)
![Page 34: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/34.jpg)
17. Which of the following has highestBoiling ?
(A) C4H9Cl (B) C4H9OH
(C) C4H9Br (D)
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17. Which of the following has highestBoiling ?
(A) C4H9Cl (B) C4H9OH
(C) C4H9Br (D) 3 2 2|CH CH CH CH OH
OH
![Page 35: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/35.jpg)
Ans: (D)Dihydric alcohols have highest B.Pt due toextensive intermolecular H-bonding
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Ans: (D)Dihydric alcohols have highest B.Pt due toextensive intermolecular H-bonding
![Page 36: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/36.jpg)
18. CH3 CH2 CH2Br
The compound Y is
(A) Propene (B) n-propylalcohol(C) propane (D) n-propyl borate
3
2 2
BHalc. KOHH O /NaOH
X Y.
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18. CH3 CH2 CH2Br
The compound Y is
(A) Propene (B) n-propylalcohol(C) propane (D) n-propyl borate
![Page 37: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/37.jpg)
I step is de hydrohalogenation and an alkeneis obtainedII step is alkene on hydroboration oxidationgives an alcohol against to markovnikov’srule.
Ans: (B)
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I step is de hydrohalogenation and an alkeneis obtainedII step is alkene on hydroboration oxidationgives an alcohol against to markovnikov’srule.
Ans: (B)
![Page 38: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/38.jpg)
19. Which of the following reagents is used inthe conversion of primary alcohol toaldehydes only?
(A)Corey’s reagent (B) Lucas reagent
(C) Baeyer’s reagent (D) Victor meyer’s reagent
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19. Which of the following reagents is used inthe conversion of primary alcohol toaldehydes only?
(A)Corey’s reagent (B) Lucas reagent
(C) Baeyer’s reagent (D) Victor meyer’s reagent
![Page 39: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/39.jpg)
Ans (A): Corey’s reagent PCC
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![Page 40: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/40.jpg)
20) The following structure onoxymercuration-reduction gives
a) b)
c) d)
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20) The following structure onoxymercuration-reduction gives
a) b)
c) d)
![Page 41: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/41.jpg)
Mark Rule
Oxymercuration –reduction reagent is Mercuric acetate in THFand water and reduction with NaBH4 which takes placeaccording to Mark Rule
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Ans: A)
![Page 42: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/42.jpg)
21)Which of the following functional groupcannot be reduced to alcohol usingsodium borohydride in ethanoic solution?
a) R – CHOb) R – CO – Rc) R – COOHd) RCOCl
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21)Which of the following functional groupcannot be reduced to alcohol usingsodium borohydride in ethanoic solution?
a) R – CHOb) R – CO – Rc) R – COOHd) RCOCl
![Page 43: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/43.jpg)
NaBH4 is a mild reducing agentNaBH4 can reduce aldehyde, ketones,acid chlorides to alcohols but not acids orethers.
Ans: c) R−COOH
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NaBH4 is a mild reducing agentNaBH4 can reduce aldehyde, ketones,acid chlorides to alcohols but not acids orethers.
Ans: c) R−COOH
![Page 44: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/44.jpg)
22) Which of the following is correct orderof solubility of alcohols in water?
A)isopropyl alcohol > n – propyl alcohol > ethylalcohol
B) isopropyl alcohol > ethyl alcohol > n – propylalcohol
C) isopropyl alcohol < n – propyl alcohol > ethylalcohol
D) n – propyl alcohol < isoporpyl alcohol < ethylalcohol
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22) Which of the following is correct orderof solubility of alcohols in water?
A)isopropyl alcohol > n – propyl alcohol > ethylalcohol
B) isopropyl alcohol > ethyl alcohol > n – propylalcohol
C) isopropyl alcohol < n – propyl alcohol > ethylalcohol
D) n – propyl alcohol < isoporpyl alcohol < ethylalcohol
![Page 45: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/45.jpg)
Branching increases solubility, straightchain alcohols are less soluble. This isdue to the surface area of non-polarhydrocarbon part decreases and solubilityincreases.
Ans:c) Isopropyl alcohol > ethylalcohol >propyl alcohols
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Branching increases solubility, straightchain alcohols are less soluble. This isdue to the surface area of non-polarhydrocarbon part decreases and solubilityincreases.
Ans:c) Isopropyl alcohol > ethylalcohol >propyl alcohols
![Page 46: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/46.jpg)
23) The order of reactivity of hydrogenhalide towards ROH is
a) HI > HBr > HCl
b) HI < HBr < HCl
c) HI > HBr < HCl
d) HI < HBr < HCl
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23) The order of reactivity of hydrogenhalide towards ROH is
a) HI > HBr > HCl
b) HI < HBr < HCl
c) HI > HBr < HCl
d) HI < HBr < HCl
![Page 47: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/47.jpg)
As we move from HCl to HBr to HI, acidstrength increases and bond strengthdecreases.
Ans: a) HI > HBr > HCl
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As we move from HCl to HBr to HI, acidstrength increases and bond strengthdecreases.
Ans: a) HI > HBr > HCl
![Page 48: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/48.jpg)
24. Which of the following reacts withsodium bicarbonate?
A) phenol B) waterC) alcohol D) picric acid.
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24. Which of the following reacts withsodium bicarbonate?
A) phenol B) waterC) alcohol D) picric acid.
![Page 49: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/49.jpg)
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is an acid stronger than H2CO3 orHCO3
-. Hence it reacts withNaHCO3 to liberate CO2.Ans: D) picric acid
![Page 50: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/50.jpg)
25. A trihydric phenol is –
A) catechol B) phloroglucinolC) quinol D) resorcinol
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25. A trihydric phenol is –
A) catechol B) phloroglucinolC) quinol D) resorcinol
![Page 51: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/51.jpg)
Ans:
B)
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![Page 52: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/52.jpg)
26.Match the acids and their pKavalues
P] p-cresol 1] 7.15Q] p-nitrophenol 2] 0.71R] phenol 3] 9.98S] picric acid 4] 10.14
A) P-4, Q-1, R-3, S-2B) P-2, Q-1, R-3, S-4C) P-3, Q-1, R-2, S-4D) P-1, Q-3,R-4, S-2
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26.Match the acids and their pKavalues
P] p-cresol 1] 7.15Q] p-nitrophenol 2] 0.71R] phenol 3] 9.98S] picric acid 4] 10.14
A) P-4, Q-1, R-3, S-2B) P-2, Q-1, R-3, S-4C) P-3, Q-1, R-2, S-4D) P-1, Q-3,R-4, S-2
![Page 53: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/53.jpg)
Cresol is weaker acid than phenol,has higher pKa value than phenol.Nitrophenol is stronger acid thanphenol, has lower pKa value. Picricacid is the strongest acid, haslowest pKa value.Ans: A) P-4, Q-1, R-3, S-2
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Cresol is weaker acid than phenol,has higher pKa value than phenol.Nitrophenol is stronger acid thanphenol, has lower pKa value. Picricacid is the strongest acid, haslowest pKa value.Ans: A) P-4, Q-1, R-3, S-2
![Page 54: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/54.jpg)
27.When phenol/salicylic acid isshaken with bromine water, thewhite precipitate formed is-
A) 2,4,6-trinitrotolueneB) 2,4,6-trinitrophenolC) 2,4,6-tribromophenolD) 2,4,6-tribromotoluene
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27.When phenol/salicylic acid isshaken with bromine water, thewhite precipitate formed is-
A) 2,4,6-trinitrotolueneB) 2,4,6-trinitrophenolC) 2,4,6-tribromophenolD) 2,4,6-tribromotoluene
![Page 55: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/55.jpg)
Both phenol and salicylic acidhave ring activating –OH group.Hence both form tribromoderivativewith bromine water.Ans: C) 2, 4, 6-tribromophenol
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Both phenol and salicylic acidhave ring activating –OH group.Hence both form tribromoderivativewith bromine water.Ans: C) 2, 4, 6-tribromophenol
![Page 56: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/56.jpg)
28.Which of the following gives atribromo derivative when treatedwith bromine water?
A) m-cresol B) o-cresolC) p-cresol D) benzyl alcohol
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28.Which of the following gives atribromo derivative when treatedwith bromine water?
A) m-cresol B) o-cresolC) p-cresol D) benzyl alcohol
![Page 57: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/57.jpg)
m-cresol is
It has all o and p positions free forbromination. Hence forms atribromo derivative.Ans: A) m-cresol
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m-cresol is
It has all o and p positions free forbromination. Hence forms atribromo derivative.Ans: A) m-cresol
![Page 58: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/58.jpg)
29. The number of alcoholic andethereal isomers possible forC4H10O are
A) 4 and 3 B) 3 and 2C) 3 and 4 D) 4 and 2
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29. The number of alcoholic andethereal isomers possible forC4H10O are
A) 4 and 3 B) 3 and 2C) 3 and 4 D) 4 and 2
![Page 59: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/59.jpg)
With C4H10O – four butyl alcoholsand 3 isomeric ethers are possible.
Ans:A) 4 and 3
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With C4H10O – four butyl alcoholsand 3 isomeric ethers are possible.
Ans:A) 4 and 3
![Page 60: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/60.jpg)
30. A compound X reacts with phthalic anhydridein presence of conc. H2SO4 forming thecompound Y which gives pink colour withNaOH solution. The compound Y is
(A)Phenol (B) Phenolphthalein(C) toluene (D) o-cresol
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30. A compound X reacts with phthalic anhydridein presence of conc. H2SO4 forming thecompound Y which gives pink colour withNaOH solution. The compound Y is
(A)Phenol (B) Phenolphthalein(C) toluene (D) o-cresol
![Page 61: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/61.jpg)
X = phenol, Y = phenolphthalein
Ans: (B)
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X = phenol, Y = phenolphthalein
Ans: (B)
![Page 62: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/62.jpg)
31. Identify the product ‘Y’.
A) benzyl alcoholB) anisoleC) benzoic acidD) benzyl methyl ether
OH
LiAlH4 XCH2N2 Y
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31. Identify the product ‘Y’.
A) benzyl alcoholB) anisoleC) benzoic acidD) benzyl methyl ether
![Page 63: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/63.jpg)
For diazomethane no catalyst isrequired.Ans:D) Benzyl methyl ether
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For diazomethane no catalyst isrequired.Ans:D) Benzyl methyl ether
![Page 64: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/64.jpg)
32. When phenol is converted to salicylaldehydeby treating it with CHCl3 and NaOH. Thereaction is called as
(A)Kolbe’s reaction(B) Friedel Crafts reaction(C) Reimer Tiemann reaction(D) Fries reaction
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32. When phenol is converted to salicylaldehydeby treating it with CHCl3 and NaOH. Thereaction is called as
(A)Kolbe’s reaction(B) Friedel Crafts reaction(C) Reimer Tiemann reaction(D) Fries reaction
![Page 65: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/65.jpg)
Reimer Tiemann reactionAns: (C)
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Reimer Tiemann reactionAns: (C)
![Page 66: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/66.jpg)
33. O-nitrophenol and p-nitrophenol areseparated by
(A) steam distillation (B) ordinary distillation(C) fractional distillation (D) solvent extraction
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33. O-nitrophenol and p-nitrophenol areseparated by
(A) steam distillation (B) ordinary distillation(C) fractional distillation (D) solvent extraction
![Page 67: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/67.jpg)
Stream distillation, more volatile O-nitrophenoldue to intra molecular H-bond gets separatedeasily.Ans:(A)
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![Page 68: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/68.jpg)
34. In the reaction3 2 2 4only AlCl O H SO
6 6 heatC H X Y Z phenol acetone
The compound Y in the above reaction is
(A) Isopropyl benzene (B) Ethyl benzene(C) Acetophenone (D) Toluene
only
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The compound Y in the above reaction is
(A) Isopropyl benzene (B) Ethyl benzene(C) Acetophenone (D) Toluene
![Page 69: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/69.jpg)
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Ans: (A)
![Page 70: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/70.jpg)
35. The compound C4H10O(X) is produced bythe reaction of conc. H2SO4 / H2O on alkene,and X is not resolvable into optical isomers.The X compound is
(A)2-methyl propan-2-ol(B) 2-methyl propan-1-ol(C) 2, 2 dimethyl ethan-1-ol(D) 2-methyl butan-2-ol
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35. The compound C4H10O(X) is produced bythe reaction of conc. H2SO4 / H2O on alkene,and X is not resolvable into optical isomers.The X compound is
(A)2-methyl propan-2-ol(B) 2-methyl propan-1-ol(C) 2, 2 dimethyl ethan-1-ol(D) 2-methyl butan-2-ol
![Page 71: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/71.jpg)
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Ans: (A)
![Page 72: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/72.jpg)
36. In the following compounds
Order of acidity is(A) (III) > IV > I > II (B) I > IV > III > II(C) II > I > III > IV (D) IV > III > I > II
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36. In the following compounds
Order of acidity is(A) (III) > IV > I > II (B) I > IV > III > II(C) II > I > III > IV (D) IV > III > I > II
![Page 73: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/73.jpg)
Ans: (D)
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![Page 74: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/74.jpg)
37. When ethoxy ethane is treated withexcess of HI at 373 K the product /products formed are
(A) C2H5OH + C2H5I (B) C2H5I(C) C2H6 + C2H5I (D) C4H10
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37. When ethoxy ethane is treated withexcess of HI at 373 K the product /products formed are
(A) C2H5OH + C2H5I (B) C2H5I(C) C2H6 + C2H5I (D) C4H10
![Page 75: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/75.jpg)
Ans: (B) C2H5I
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38. Diethyl ether is not isomeric with
A) butanalB) 2-butanolC) methyl n-propyl etherD) buta-1-ol
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38. Diethyl ether is not isomeric with
A) butanalB) 2-butanolC) methyl n-propyl etherD) buta-1-ol
![Page 77: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/77.jpg)
For C2H5OC2H5 ; CH3CH2CH2CH2OH,CH3CH(OH)CH2CH3 andCH3O-CH2CH2CH3 are all isomersbut not CH3CH2CH2CHO (butanal)
Ans: A) butanal
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For C2H5OC2H5 ; CH3CH2CH2CH2OH,CH3CH(OH)CH2CH3 andCH3O-CH2CH2CH3 are all isomersbut not CH3CH2CH2CHO (butanal)
Ans: A) butanal
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39. dibenzyl ether is heated with (a)1mole HI and (b) excess HI theproducts formed are
a bA 2molC6H5CH2OH C6H5CH2OH+C6H5CH2I
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A 2molC6H5CH2OH C6H5CH2OH+C6H5CH2I
B C6H5CH2OH+C6H5CH2I 2mol C6H5CH2IC 2mol C6H5CH2I C6H5CH2OH+C6H5CH2I
D 2mol C6H5CH2I 2mol C6H5CH2OH
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Ans:B) C6H5CH2OH + C2H5CH2I,
2 mol C6H5CH2I
![Page 80: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/80.jpg)
40. Aspirin is the acetylated product of
A) o-hydroxybenzoic acidB) o-hydroxy benzeneC) m-hydroxybenzoicacidD) o-hydroxybenzaldehyde
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40. Aspirin is the acetylated product of
A) o-hydroxybenzoic acidB) o-hydroxy benzeneC) m-hydroxybenzoicacidD) o-hydroxybenzaldehyde
![Page 81: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/81.jpg)
is aspirin, obtained by acetylation of
o-hydroxy benzoic acidAns: A) o-hydroxybenzoic acid
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is aspirin, obtained by acetylation of
o-hydroxy benzoic acidAns: A) o-hydroxybenzoic acid
![Page 82: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/82.jpg)
41. 2-phenylethanol is preparedusing
A) phenyl magnesium bromide andethylene oxide
B) phenyl magnesium bromide andethylene glycol
C) phenyl magnesium bromide andethyl alcohol
D) methyl magnesium bromide andbenzaldehyde
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41. 2-phenylethanol is preparedusing
A) phenyl magnesium bromide andethylene oxide
B) phenyl magnesium bromide andethylene glycol
C) phenyl magnesium bromide andethyl alcohol
D) methyl magnesium bromide andbenzaldehyde
![Page 83: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/83.jpg)
C6H5CH2CH2OH is 2-phenylethanol(2) (1)
Ans: A) Phenyl magnesium bromideand ethylene oxide
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C6H5CH2CH2OH is 2-phenylethanol(2) (1)
Ans: A) Phenyl magnesium bromideand ethylene oxide
![Page 84: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/84.jpg)
42. Identify the products formedwhen t-butyl methyl ether isheated with limited conc.HI
A) t-butyl alcohol & methyl iodideB) t-butyl iodide & methyl alcoholC) t-butyl iodide & methyl iodideD) t-butyl alcohol & methyl alcohol
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42. Identify the products formedwhen t-butyl methyl ether isheated with limited conc.HI
A) t-butyl alcohol & methyl iodideB) t-butyl iodide & methyl alcoholC) t-butyl iodide & methyl iodideD) t-butyl alcohol & methyl alcohol
![Page 85: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/85.jpg)
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Ans:b) t-butyliodide and methyl alcohol
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43. In the reaction
The products A and B respectively are
(A)Iodobenzene and methanol(B) Phenol and Iodomethane(C) Benzene and Methoxy iodide(D) Benzene and methanol
373 K6 5 3C H OCH HI A B
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43. In the reaction
The products A and B respectively are
(A)Iodobenzene and methanol(B) Phenol and Iodomethane(C) Benzene and Methoxy iodide(D) Benzene and methanol
![Page 87: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/87.jpg)
The bond between -O-CH3 is weaker than-O-C6H5 because in-O-C6H5 the carbon group issp2 hybridised and oxygen attains partial doublebond character through resonance.
Ans: (B) Phenol and Iodomethane
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The bond between -O-CH3 is weaker than-O-C6H5 because in-O-C6H5 the carbon group issp2 hybridised and oxygen attains partial doublebond character through resonance.
Ans: (B) Phenol and Iodomethane
![Page 88: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/88.jpg)
44. During the reactionThe main product A is
(A) Isobutene (B) tes butyl ether(C) Isobutane (D) ter butyl ether
3 3 3(CH ) C Cl CH ONa A
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For the preparation of unsymmetrical ethers,the alkyl halides should be primary, whereasthe alkoxides may be 1, 2 or 3. Ether isnot formed. Elimination competes oversubstitution reaction. Hence the answer isAns: (A) Isobutene
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For the preparation of unsymmetrical ethers,the alkyl halides should be primary, whereasthe alkoxides may be 1, 2 or 3. Ether isnot formed. Elimination competes oversubstitution reaction. Hence the answer isAns: (A) Isobutene
![Page 90: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/90.jpg)
45. During the Friedel crafts reaction ofanisole with acetyl chloride in presence ofanhy AlCl3, the major product obtained is
(A)m-methoxy acetophenone(B) o-methoxy acetophenone(C) p-methoxy acetophenone(D) p-methylanisole
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45. During the Friedel crafts reaction ofanisole with acetyl chloride in presence ofanhy AlCl3, the major product obtained is
(A)m-methoxy acetophenone(B) o-methoxy acetophenone(C) p-methoxy acetophenone(D) p-methylanisole
![Page 91: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/91.jpg)
Ans: (C) p-methoxy acetophenone
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Ans: (C) p-methoxy acetophenone
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46. What is the major product obtained when
(A)
(B)
(C)
(D)
is heated
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46. What is the major product obtained when
(A)
(B)
(C)
(D)
![Page 93: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/93.jpg)
C6H4 (OH)-O- bond is stronger bond than theother group. Hence the bond is C6H4 (OH)-O- isnot cleaved.
Ans: (A)
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C6H4 (OH)-O- bond is stronger bond than theother group. Hence the bond is C6H4 (OH)-O- isnot cleaved.
Ans: (A)
![Page 94: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/94.jpg)
47. Match the structures of the compounds given inColumn I with the name of the compounds given in ColumnII. Column I
(i)
(ii)
(iii)
(iv)
(v)
Column II(a) Hydroquinone
(b) Catechol
(c) o-Cresol
(d) Quinone(e)Resorcinol(f) Anisole
(i)
(ii)
(iii)
(iv)
(v)
(a) Hydroquinone
(b) Catechol
(c) o-Cresol
(d) Quinone(e)Resorcinol(f) Anisole
![Page 95: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/95.jpg)
48. Match the items of column I with items of column II.
Column I Column II
(i)Antifreeze used in car engine
(ii) Solvent used in perfumes
(iii) Starting material for picricacid
(iv) Wood spirit
(v) Reagent used for detectionof phenols
(vi) By product of soap industry
(a) Neutral ferric chloride
(b) Glycerol
(c) Methanol
(d) Phenol
(e) Ethleneglycol phenolicgroup
(f) Ethanol used incosmetics
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(i)Antifreeze used in car engine
(ii) Solvent used in perfumes
(iii) Starting material for picricacid
(iv) Wood spirit
(v) Reagent used for detectionof phenols
(vi) By product of soap industry
(a) Neutral ferric chloride
(b) Glycerol
(c) Methanol
(d) Phenol
(e) Ethleneglycol phenolicgroup
(f) Ethanol used incosmetics
![Page 96: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/96.jpg)
49. The compound which is also known ascarbolic acid is
(A)Phenol (B) Benzene(C) cresol (D) Toluene
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49. The compound which is also known ascarbolic acid is
(A)Phenol (B) Benzene(C) cresol (D) Toluene
![Page 97: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/97.jpg)
Ans: A) Phenol
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50. The IUPAC name of m-Cresol is
(A) 3-chlorophenol (B) 3-Methoxyphenol
(C) 3-methyl phenol (D) benzene -1, 3-diol
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50. The IUPAC name of m-Cresol is
(A) 3-chlorophenol (B) 3-Methoxyphenol
(C) 3-methyl phenol (D) benzene -1, 3-diol
![Page 99: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/99.jpg)
Ans: (C) 3-methyl phenol
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51.In the following reaction:
The compound E in the reaction?
(A)Benzene (B) Phenol(C) Cyclohexanol (D) Cyclohexane
2H /NiZn Oleum NaOH HClNaOH 573 K
A B C D E
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51.In the following reaction:
The compound E in the reaction?
(A)Benzene (B) Phenol(C) Cyclohexanol (D) Cyclohexane
![Page 101: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/101.jpg)
Benzene on fusion with Oleum and NaOH givesSod. Benzene Sulphonate
Ans: (C) Cyclohexanol
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Benzene on fusion with Oleum and NaOH givesSod. Benzene Sulphonate
Ans: (C) Cyclohexanol
![Page 102: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/102.jpg)
52.Phenol condenses with HCHO in thepresence of dil acid to form the polymer
(A)Bakelite (B) Buna-S(C) Teflon (D) Melamine
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52.Phenol condenses with HCHO in thepresence of dil acid to form the polymer
(A)Bakelite (B) Buna-S(C) Teflon (D) Melamine
![Page 103: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/103.jpg)
Ans(A) Bakelite
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53. How will you distinguish between phenoland Benzyl alcohol?
(A)using neutral FeCl3(B) using acidic FeCl3(C) using neutral FeCl2(D) using acidic FeCl2
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53. How will you distinguish between phenoland Benzyl alcohol?
(A)using neutral FeCl3(B) using acidic FeCl3(C) using neutral FeCl2(D) using acidic FeCl2
![Page 105: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/105.jpg)
All phenols give violet colour with neutralFeCl3.Fe(C6H5O)3 is violet in colour.
Ans: (A)
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All phenols give violet colour with neutralFeCl3.Fe(C6H5O)3 is violet in colour.
Ans: (A)
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54. When phenol reacts with Br2 in CS2 at 0C,the major product obtained is
(A) 2-bromo phenol (B) 3-bromo phenol(C) 4-bromo phenol (D) 2, 4, 6 tribromo phenol
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54. When phenol reacts with Br2 in CS2 at 0C,the major product obtained is
(A) 2-bromo phenol (B) 3-bromo phenol(C) 4-bromo phenol (D) 2, 4, 6 tribromo phenol
![Page 107: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/107.jpg)
Ans (C): 4-bromo phenol
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55. The reaction of CH3CH = CH OHwith HBr gives
(A)CH3CHBrCH2 OH(B) CH3 CH2CHBr OH(C) CH3CHBrCH2 Br(D) CH3CH2CHBr Br
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55. The reaction of CH3CH = CH OHwith HBr gives
(A)CH3CHBrCH2 OH(B) CH3 CH2CHBr OH(C) CH3CHBrCH2 Br(D) CH3CH2CHBr Br
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Ans: (B)
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56. The IUPAC name of the etherCH3OCH(CH3)2
(A)1-methoxy propane(B) propoxy methane(C) 2-methoxy propane(D) isopropoxy methane
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56. The IUPAC name of the etherCH3OCH(CH3)2
(A)1-methoxy propane(B) propoxy methane(C) 2-methoxy propane(D) isopropoxy methane
![Page 111: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/111.jpg)
Ans: (C) 2-methoxy propane
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57. The reactants required for the preparationof ter-butyl ethyl ether by Williamson’sreaction are
(A) ter butyl chloride + sodium ethoxide(B) sodium ter butoxide + ethyl chloride(C) ter butyl alcohol + ethyl chloride(D) ethyl alcohol + ter. butyl chloride
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57. The reactants required for the preparationof ter-butyl ethyl ether by Williamson’sreaction are
(A) ter butyl chloride + sodium ethoxide(B) sodium ter butoxide + ethyl chloride(C) ter butyl alcohol + ethyl chloride(D) ethyl alcohol + ter. butyl chloride
![Page 113: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/113.jpg)
Ans: (B) sodium ter butoxide + ethyl chloride
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58) Alcohol are obtained from alkenes by
a) hydrolysis with dilute H2SO4
b) hydration with aqueous KOH
c) hydration with alkaline KMnO4
d) Hydration using conc. H2SO4 and hydrolysis
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58) Alcohol are obtained from alkenes by
a) hydrolysis with dilute H2SO4
b) hydration with aqueous KOH
c) hydration with alkaline KMnO4
d) Hydration using conc. H2SO4 and hydrolysis
![Page 115: Alcohols, Phenols & Ethers - Karnataka …kea.kar.nic.in/cet2014/vikasana/chemistry/day_13.pdfGrignard reagent followed by hydrolysis? (A) acetone (B)methyl cyanide (C) ethylene oxide](https://reader031.vdocuments.us/reader031/viewer/2022020215/5b822e0e7f8b9ae97b8ddda4/html5/thumbnails/115.jpg)
Alkenes alcohol is by hydration usingconcentrated H2SO4 and hydrolysis.
Ans: d) Hydration using conc. H2SO4 andhydrolysis
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Alkenes alcohol is by hydration usingconcentrated H2SO4 and hydrolysis.
Ans: d) Hydration using conc. H2SO4 andhydrolysis
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59) A reaction between alcohol and organicacid to form ester involves
a) the cleavage of O – H bond of acidb) the cleavage of C–O bond of alcoholc) the formation of bond between oxygen
of COO group of acid and carbon ofalcohol
d) the cleavage of C–OH bond of acid
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59) A reaction between alcohol and organicacid to form ester involves
a) the cleavage of O – H bond of acidb) the cleavage of C–O bond of alcoholc) the formation of bond between oxygen
of COO group of acid and carbon ofalcohol
d) the cleavage of C–OH bond of acid
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Ans:d) Cleavage of C−OH bond of the acid
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Ans:d) Cleavage of C−OH bond of the acid
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60)When phenyl magnesium bromidereacts with t-butanol the productwould be
a) benzeneb) phenolc) t-butyl benzened) t-butyl phenyl ether
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60)When phenyl magnesium bromidereacts with t-butanol the productwould be
a) benzeneb) phenolc) t-butyl benzened) t-butyl phenyl ether
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(CH3)3C−OH reacts with C6H5MgBr toform benzene, because the alcohol hasacidic H atom in its –OH group.
Ans: A) benzene
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(CH3)3C−OH reacts with C6H5MgBr toform benzene, because the alcohol hasacidic H atom in its –OH group.
Ans: A) benzene
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61) The compound which gives the moststable carbocation on dehydration is
A) B)
C) D)
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61) The compound which gives the moststable carbocation on dehydration is
A) B)
C) D)
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3° carbocations are the most stable.
Ans:B) (CH3)3C−OH
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3° carbocations are the most stable.
Ans:B) (CH3)3C−OH
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62) pent-3-en-2-ol is converted intopent-3-en-2-one when treated with
a) Jones’ reagent
b) potassium dichromate
c) potassium permanganate
d) LiAlH4
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62) pent-3-en-2-ol is converted intopent-3-en-2-one when treated with
a) Jones’ reagent
b) potassium dichromate
c) potassium permanganate
d) LiAlH4
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This reaction is done by using Jonesreagent.
Ans: a) Jones reagent
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This reaction is done by using Jonesreagent.
Ans: a) Jones reagent
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63) The order of dehydration of followingalcohols is
i) ii)
iii) iv)
A) I < II < III < IV B) I > II > III > IV
C) III < II < I < IV D) II < III < IV < I
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63) The order of dehydration of followingalcohols is
i) ii)
iii) iv)
A) I < II < III < IV B) I > II > III > IV
C) III < II < I < IV D) II < III < IV < I
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Allylic and 3° alcohols undergodehydration the fastest.
Ans: c) III < II < I < IV
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Allylic and 3° alcohols undergodehydration the fastest.
Ans: c) III < II < I < IV
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64) Hydrogen bonding is maximum in
A) ethanol
B) diethyl ether
C) ethylchloride
D) triethylamine
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64) Hydrogen bonding is maximum in
A) ethanol
B) diethyl ether
C) ethylchloride
D) triethylamine
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Ans: a) Ethanol
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Ans: a) Ethanol
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65) The dehydration of butanol–2 gives
A. 1 – butene onlyB. 2 – butene onlyC. both 1 – butene and 2 – butene
with 1–butene as major productD. both 1 – butene and 2 – butene
with 2–butene as major product128
65) The dehydration of butanol–2 gives
A. 1 – butene onlyB. 2 – butene onlyC. both 1 – butene and 2 – butene
with 1–butene as major productD. both 1 – butene and 2 – butene
with 2–butene as major product
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Ans:
d) both 1 – butene and 2 – butene with2 – butene as major product
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Ans:
d) both 1 – butene and 2 – butene with2 – butene as major product
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66) A mixture of methanol vapour and airis passed over heated copper. Theproducts are
A) carbon monoxide and hydrogenB) formaldehyde and water vapourC) formic acid and water vapourD) carbon monoxide and water vapour
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66) A mixture of methanol vapour and airis passed over heated copper. Theproducts are
A) carbon monoxide and hydrogenB) formaldehyde and water vapourC) formic acid and water vapourD) carbon monoxide and water vapour
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OHCHOHOOHCH 2Cu
23
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Ans:
b) formaldehyde and water vapour
OHCHOHOOHCH 2Cu
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67). Which of these is not a productof phenol?
A) bakelite B) phenolphthaleinC) paracetamol D) melamine
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67). Which of these is not a productof phenol?
A) bakelite B) phenolphthaleinC) paracetamol D) melamine
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Ans:
D) Melamine
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Ans:
D) Melamine
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68).(a) di n-propyl ether ismanufactured by heating n-propylalcohol with conc. H2SO4.(b) di isopropylether cannot beobtained in the same way becauseelimination takes place to givealkenes.A) A is true, B is wrongB) A is wrong, B is trueC) both are true D)both are wrong
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68).(a) di n-propyl ether ismanufactured by heating n-propylalcohol with conc. H2SO4.(b) di isopropylether cannot beobtained in the same way becauseelimination takes place to givealkenes.A) A is true, B is wrongB) A is wrong, B is trueC) both are true D)both are wrong
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Ans: C) both are trueBecause n-propyl alcohol is 1°alcohol. Isopropyl alcohol is 2°alcohol.
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Ans: C) both are trueBecause n-propyl alcohol is 1°alcohol. Isopropyl alcohol is 2°alcohol.
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69). To get cresol, phenol issubjected to
A) Wurtz reactionB) Fittig reactionC)Friedel-Crafts reactionD)Gatterman reaction
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69). To get cresol, phenol issubjected to
A) Wurtz reactionB) Fittig reactionC)Friedel-Crafts reactionD)Gatterman reaction
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Ans: C)Friedel-Craft’s reaction
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70). C7H8O could be which of thefollowing?
i] cresol ii] benzyl alcoholiii] anisole iv] toluidine
A) i, ii, iii B) ii, iiiC) ii, iii, iv D) i, ii, iv
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70). C7H8O could be which of thefollowing?
i] cresol ii] benzyl alcoholiii] anisole iv] toluidine
A) i, ii, iii B) ii, iiiC) ii, iii, iv D) i, ii, iv
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C7H8O can be
Ans: a) i, ii, iii
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C7H8O can be
Ans: a) i, ii, iii
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71). A compound ‘X’ with molecular formulaC3H8O can be oxidized to a compoundwith molecular formula C3H6O2. ‘X’ ismost likely a/an
(A)primary alcohol(B)secondary alcohol(C) Aldehyde(D) ketone
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71). A compound ‘X’ with molecular formulaC3H8O can be oxidized to a compoundwith molecular formula C3H6O2. ‘X’ ismost likely a/an
(A)primary alcohol(B)secondary alcohol(C) Aldehyde(D) ketone
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Ans: (A)
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72).Which is not a phenol –
A) aspirinB)salicylic acidC) phenyl salicylate (salol)D) naphthol
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72).Which is not a phenol –
A) aspirinB)salicylic acidC) phenyl salicylate (salol)D) naphthol
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is aspirin it is not a phenol.Ans: A) Aspirin
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is aspirin it is not a phenol.Ans: A) Aspirin
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Wish you all the best
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