From the picture and description can you is that a correct mechanism . can you draw the mechanism ?Phosphate Ester (Minor Product):In the mechanism, a nucleophilic attack by the phosphate ion (�2��4−H2PO4−) substitutes the hydroxyl group in the protonated cyclohexanol.This is a minor product due to steric hindrance. The phosphate group is relatively large and bulky, making the substitution reaction less favored. The size of the substituent may lead to a slower reaction rate and decreased likelihood of successful substitution.Ether (Minor Product):In the mechanism, substitution involves another cyclohexanol molecule attacking the hydroxyl group in the protonated cyclohexanol.Steric hindrance and the availability of a more favorable elimination pathway (dehydration) contribute to the ether being a minor product. The proximity of two cyclohexanol molecules for substitution is hindered by steric factors, making elimination more favorable. 1. Phosphate Ester Formation:C6H11OH2+ + H2PO4-2. Ether Formation:SubstitutionC6H11OH2+ + C6H110HC6H11OP (O)(OH)2 + H3O+SubstitutionC6H11OC6H11 + H3O+

A reaction is a process by which the reactants are converted to the product. The mechanism gives the…

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Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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From the picture and description can you is that a correct mechanism . can you draw the mechanism ?

Phosphate Ester (Minor Product):
- In the mechanism, a nucleophilic attack by the phosphate ion (�2��4−H2PO4−) substitutes the hydroxyl group in the protonated cyclohexanol.
- This is a minor product due to steric hindrance. The phosphate group is relatively large and bulky, making the substitution reaction less favored. The size of the substituent may lead to a slower reaction rate and decreased likelihood of successful substitution.
Ether (Minor Product):
- In the mechanism, substitution involves another cyclohexanol molecule attacking the hydroxyl group in the protonated cyclohexanol.
- Steric hindrance and the availability of a more favorable elimination pathway (dehydration) contribute to the ether being a minor product. The proximity of two cyclohexanol molecules for substitution is hindered by steric factors, making elimination more favorable.

1. Phosphate Ester Formation:
C6H11OH2+ + H2PO4-
2. Ether Formation:
Substitution
C6H11OH2+ + C6H110H
C6H11OP (O)(OH)2 + H3O+
Substitution
C6H11OC6H11 + H3O+

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