Describe what happen in each step as specific as possible. 1. What is La Chatelier ‘s principle？how it contribute to Fischer Esterification？2. Explain the mechanism ，what happen in each reaction？ Fischer Esterification.utilizes La chatelier's principle to shift theequilibrium.CH3COacetic acidMechanismOHCH3-C=0.productCO=C:ÖYOHCH₂-C-ÖR+ H₂SO4+монisopentyl alcohol(bad smell)24H2804: HITSCH3-C-OH1804HSO4 +CH3-C-ÖR:O:H TH=0CH3-Cisopentyl acetate-H0.CH3-C-OHLoss ofH₂0Xalcohol+4₂00-0-0:+0:3:9-HCHS-C-OHR-O:11HCH₂-CHalicHeintramoletransforC

Describe what happen in each step as specific as possible. 1. What is La Chatelier ‘s principle？how it contribute to Fischer Esterification？ 2. Explain the mechanism ，what happen in each reaction？

Describe what happen in each step as specific as possible. 1. What is La Chatelier ‘s principle？how it contribute to Fischer Esterification？ 2. Explain the mechanism ，what happen in each reaction？

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter20: Carboxylic Acids And Nitriles

Section20.2: Structure And Properties Of Carboxylic Acids

Problem 4P: The Ka for dichloroacetic acid is 3.32 Ă— 10-2. Approximately what percentage of the acid is...

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Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.

Question

Fischer Esterification.
utilizes La chatelier's principle to shift the
equilibrium.
CH3CO
acetic acid
Mechanism
OH
CH3-C=0.
product
CO=C
:Ö
YOH
CH₂-C-ÖR
+ H₂SO4
+
мон
isopentyl alcohol
(bad smell)
24
H2804
: H
ITS
CH3-C-OH
1804
HSO4 +
CH3-C-ÖR
:O:
H TH
=0
CH3-C
isopentyl acetate
-H
0.
CH3-C-OH
Loss of
H₂0
X
alcohol
+4₂0
0-0-0:
+0:3
:9-H
CHS-C-OH
R-O:
11
H
CH₂-CH
alic
H
e
intramole
transfor
C

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