(b) The reaction (R)-2-chloro-3-methylbutane with KOH shown below, resulted in a mixture of three alcohols: W and its enantiomer X and compound Y. H3C CH3 H3C он H7 H3C кон Ethanol + Enantiomer X + Y CI H3C CH3 (R)-2-chloro-3-methylbutane (1) Deduce the structures of compounds X and Y and assign the stereochemistry for compounds W and X. (i) Use reaction mechanisms to account for the formation of the MAJOR product.

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(b) The reaction (R)-2-chloro-3-methylbutane with KOH shown below, resulted in a mixture of
three alcohols: W and its enantiomer X and compound Y.
H3C
CH3
H3C
он
Кон
Ethanol
+ Enantiomer X + Y
H
H3C
H3C
CH3
W
(R)-2-chloro-3-methylbutane
(i) Deduce the structures of compounds X and Y and assign the stereochemistry for compounds
W and X.
(i) Use reaction mechanisms to account for the formation of the MAJOR product.
Transcribed Image Text:(b) The reaction (R)-2-chloro-3-methylbutane with KOH shown below, resulted in a mixture of three alcohols: W and its enantiomer X and compound Y. H3C CH3 H3C он Кон Ethanol + Enantiomer X + Y H H3C H3C CH3 W (R)-2-chloro-3-methylbutane (i) Deduce the structures of compounds X and Y and assign the stereochemistry for compounds W and X. (i) Use reaction mechanisms to account for the formation of the MAJOR product.
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