chem lab exam tips 2.ppt. sodium fusion(lassaignes) test the organic compound to be tested is fused...
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CHEM LAB
Exam Tips 2.ppt
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SODIUM FUSION(LASSAIGNES) TEST
THE ORGANIC COMPOUND TO BE TESTED IS FUSED WITH METALLIC SODIUM.IN THIS WAY SODIUM CYANIDE,SODIUM SULPHIDE AND/OR SODIUM HALIDES IS FORMED WHICH CAN BE READILY IDENTIFIED.
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TEST FOR NITROGEN
THE CYANIDE FORMED CAN BE DETECTED BY PRUSSIAN BLUE TEST.
STEP 1: FESO4 + 6NACN=Na4[Fe(CN)6]+Na2SO4
STEP 2: 3Na4[Fe(CN)6] + 2Fe2(SO4)3=Fe4[Fe(CN)6]3(PRUSSIAN BLUE)+6Na2SO4
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TEST FOR SULPHUR
THIS IS TESTED AS SULPHIDE TEST 1: THE COMPOUND IS TREATED WITH DIL. ACETIC ACID AND
THEN WITH LEAD ACETATE.A BLACK PRECEPATE OF LEAD ACETATE INDICATES THE
PRESENCE OF SULPHUR
TEST 2:THE COMPOPUND IS TREATED WITH DIL.SOLN. OF
Na2[Fe(CN)5NO] A PURPLE COLOURED COMP. OF Na4[Fe(CN)5NOS] IS FORMED INDICATING THE PRESENCE OF SULPHUR.
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TEST FOR HALOGENS
THE FUSION SOLN IS ACIDIFIED WITH DIL.HNO3 AND THEN EXCESS OF AgNO3 IS ADDED.
COLOUR SOLUBILITY IN Aq. Ammonia
HALOGEN
WHITE COMPLETELY SOLUBLE
Cl
PALE YELLOW
PARTIAL SOL.
Br
YELLOW IN SOLUBLE. I
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_OH (ALCOHOLIC)
TEST 1::SODIUM TEST 2ROH+2Na=2RONa+H2(GAS) TEST 2:: ACETYL CHLORIDE TEST
acetyl chloride reacts vigorously with primary and secondary alcohols with evolution of HCl.
HCl +NH4OH =NH4Cl(WHITE FUMES)+ H2O
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PHENOL
GIVES VIOLET COLOUR WITH FeCl3 SOLN.
FeCl3+6C6H5OH= [Fe(OC6H5)6]-3+3HCl
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CARBONYL TEST
FOR ALDEHYDES AND KETONES.
2,4-DINITROPHENYL HYDRAZINE-TEST
-> FORMATION OF CRYSTALLINE PRECIPITATE WITH THE REAGENT INDICATES THE PRESENCE OF ALDEHYDES AND KETONES.
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SPECIFIC FOR ALDEHYDES
SCHIFF’S TEST
->APPEARANCE OF PINK RED OR MAGENTA COLOR WITH REAGENT.
TOLLEN’S TEST ->SILVER MIRROR WITH REAGENT(Ag+).
FEHLING’S TEST ->RED PRECIPITATE OF Cu2O WITH ALDEHYDE GROUP.
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CARBOXYLIC GROUP
LITMUS TEST (BLUE TO RED). SODIUM BICARBONATE
TEST(NaHCO3).CO2 MOVES OUT FROM NaHCO3.
ESTER TEST: REACTS WITH ALCOHOL TO GIVE SWEET SMELLING COMPOUND(ESTER).
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ALIPHATIC AMINO GROUP
WITH HNO2 PRIMARY GROUP GIVES ALCOHOL
WITH HNO2 SEC GIVES NITROSOAMINES YELLOW OILY LIQUID(R2N-NO).
WITH HNO2 TERTIARY GROUP GIVES TRIALKYLAMMONIUM NITRITE (R3 N+ HONO-)
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AROMATIC AMINES
WITH HNO2 PRIMARY GIVES BENZENE DIAZONIUM CHLORIDES(PhN2+ Cl-).
SECONDARY GROUP GIVES N-ALKYL-N-PHENYL NITROSOAMINE.
TERTIARY GROUP GIVES P-NITROSOANILINE.
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SPECIFIC FOR PRIMARY AMINE(ALI+ARO) UNPLEASANT ODOUR OF ISOCYNIDE(RNC) WITH CHLOROFORM+KOH.
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NITRO GROUP
THE PRESENCE OF NITRO GROUP CAN BE DETYECTED BY REDUCING THE COMPOUND WITH Sn/HCl AND THEN CONDUCTING CARBYL AMINE TEST.