Zaitsev product formed when [tex]{\mathbf{2,3 - dimethylpentan - 3 - ol}}[/tex] undergoes dehydration is drawn in the attached image.
Further Explanation:
In the elimination reaction, a pair of groups are eliminated from the molecule by a dehydrating agent such as [tex]{{\text{H}}_{\text{2}}}{\text{S}}{{\text{O}}_{\text{4}}}[/tex] or [tex]{{\text{P}}_{\text{2}}}{{\text{O}}_{\text{5}}}[/tex]. Removal of either an alkyl halide or water molecule may occur ant it results in formation of an alkene. The formation of major and minor alkene is governed by the Hoffman rule or Zaitsev rule.
There are two kinds of elimination reactions namely E1 and E2. The unimolecular elimination reactions proceed through two steps that involve carbocation formation and rearrangement. The product is governed by the pathway that leads to more stable carbocation.
Zaitsev rule says that a formation of a more substituted alkene is more favored in an elimination reaction while the Hoffman rule predicts that a least substituted alkene is more favored if the alkene is formed from asymmetrically amines such as quaternary ammonium salt.
The usual dehydration reaction of alcohol follows the Zaitsev rule. More substituted alkene is the major product formed from the elimination of water from [tex]{\text{2,3 - dimethylpentan - 3 - ol}}[/tex]. (Refer to the attached image).
Learn more:
1. Best cleaning agent for burned-on grease: https://brainly.com/question/3789105
2. The main purpose of conducting experiments: https://brainly.com/question/5096428
Answer details:
Grade: Senior School
Subject: Chemistry
Chapter: Redox reactions
Keywords: elimination reaction, Loss of water molecule, dehydration, alkene, E 1 elimination, unimolecular, Zaitsev rule, carbocation, quaternary ammonium salt, and Hoffman rule.
