The reaction between 3-bromo-4-methylhexane acetone (solvent) gives two products B (major) and C. H (A) and NaOH at high temperature in HCC C₂H5 C₂H5 H Br 1- Give the absolute configuration of asymmetric carbon in compound (A). 2- Give the structure of (B) and (C). 3- Give the mechanism that allows the formation of (B).

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The reaction between
3-bromo-4-methylhexane
acetone (solvent) gives two products B (major) and C.
H3C
H
(A) and NaOH at high temperature in
C₂H5
Br
H
1- Give the absolute configuration of asymmetric carbon in compound (A).
2- Give the structure of (B) and (C).
3- Give the mechanism that allows the formation of (B).
Transcribed Image Text:The reaction between 3-bromo-4-methylhexane acetone (solvent) gives two products B (major) and C. H3C H (A) and NaOH at high temperature in C₂H5 Br H 1- Give the absolute configuration of asymmetric carbon in compound (A). 2- Give the structure of (B) and (C). 3- Give the mechanism that allows the formation of (B).
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