Compound AA, C4H8O, gives a positive result (formation of a silver mirror) when reacted with Tollen’s reagent. Reduction of compound AA with lithium aluminium hydride, LiAlH4 followed by acidified water, H3O+ produces an alcohol, BB. Oxidation of BB with hot acidified potassium dichromate, K2Cr2O7 gives butanoic acid, C3H7COOH. Esterification between butanoic acid and methanol, CH3OH produces compound CC. Dehydration of compound BB using concentrated sulphuric acid, H2SO4 at a temperature of 180°C produces compound DD. Draw the structural formula of compounds AA, BB, CC, and DD
Compound AA, C4H8O, gives a positive result (formation of a silver mirror) when reacted with Tollen’s reagent. Reduction of compound AA with lithium aluminium hydride, LiAlH4 followed by acidified water, H3O+ produces an alcohol, BB. Oxidation of BB with hot acidified potassium dichromate, K2Cr2O7 gives butanoic acid, C3H7COOH. Esterification between butanoic acid and methanol, CH3OH produces compound CC. Dehydration of compound BB using concentrated sulphuric acid, H2SO4 at a temperature of 180°C produces compound DD. Draw the structural formula of compounds AA, BB, CC, and DD
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter17: Carboxylic Acids
Section: Chapter Questions
Problem 17.43P
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7. Compound AA, C4H8O, gives a positive result (formation of a silver mirror) when reacted with Tollen’s reagent. Reduction of compound AA with lithium aluminium hydride, LiAlH4 followed by acidified water, H3O+ produces an alcohol, BB. Oxidation of BB with hot acidified potassium dichromate, K2Cr2O7 gives butanoic acid, C3H7COOH. Esterification between butanoic acid and methanol, CH3OH produces compound CC. Dehydration of compound BB using concentrated sulphuric acid, H2SO4 at a temperature of 180°C produces compound DD.
Draw the structural formula of compounds AA, BB, CC, and DD
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