Fischer Esterification is a reversible reaction. How do we ensure that the formation of the product is more favored? Using only a small amount of the alcohol Using an excess of reactants Using heat Using mineral oil to separate the product from the unreacted reactants Previous

Fischer Esterification is a reversible reaction. How do we ensure that the formation of the product is more favored? Using only a small amount of the alcohol Using an excess of reactants Using heat Using mineral oil to separate the product from the unreacted reactants Previous

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 2E

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Question

7 8

Fischer Esterification is a reversible reaction. How do we ensure that the formation of the product is more favored?
Using only a small amount of the alcohol
Using an excess of reactants
Using heat
Using mineral oil to separate the product from the unreacted reactants
Previous

What is the relationship between the two compounds shown below?
Br
Diastereomers
Constitutional isomers
Enantiomers
Identical
Previous
Br
OH
and
HO
Br
Br

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