Aldehyde and ester mixed with sodium ethooxide in ethanol produces 4 possible products. Please draw the other 3 products with unique carbon skeletons. C12H1602OH OH.1) NaOEt,ELOHBr4 possible products with unique carbon skeletons(not counting diastereomers and enantiomers)2) mild acidicworkup(to neutralizeNaOEt)BrC18H16B1203

Detail mechanistic pathway is given below to find out the other products

Answered: C12H1602 OH O H. 1) NaOEt, ELOH Br 4…

C12H1602 OH O H. 1) NaOEt, ELOH Br 4 possible products with unique carbon skeletons (not counting diastereomers and enantiomers) 2) mild acidic workup (to neutralize NaOEt) Br C18H16B1203

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter5: Stereochemistry At Tetrahedral Centers

Section5.SE: Something Extra

Problem 62AP

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Question

Aldehyde and ester mixed with sodium ethooxide in ethanol produces 4 possible products. Please draw the other 3 products with unique carbon skeletons.

C12H1602
OH O
H.
1) NaOEt,
ELOH
Br
4 possible products with unique carbon skeletons
(not counting diastereomers and enantiomers)
2) mild acidic
workup
(to neutralize
NaOEt)
Br
C18H16B1203

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

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