Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas.

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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Please answer BOTH questions, thanks so much!
H3CO
1. LIAIH4, THF
2. H3O+ quench
Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. Show the appropriate stereochemistry by choosing the dashed
or wedged buttons and then clicking a bond on the canvas.
H: 120 EXP
&
Marvin JS
ChemAxon
I UZOJ -
P
Transcribed Image Text:H3CO 1. LIAIH4, THF 2. H3O+ quench Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas. H: 120 EXP & Marvin JS ChemAxon I UZOJ - P
Classify the following nucleophiles as strong, weak, or intermediate.
Drag the appropriate nucleophiles to their respective bins.
Strong nucleophile
O
LOH
Na CN
Weak nucleophile
MgBr
Intermediate nucleophile
Reset
Transcribed Image Text:Classify the following nucleophiles as strong, weak, or intermediate. Drag the appropriate nucleophiles to their respective bins. Strong nucleophile O LOH Na CN Weak nucleophile MgBr Intermediate nucleophile Reset
Expert Solution
Step 1

LiAlH4 is a strong reducing agent which reduces carbonyl compounds (ketones, aldehydes, esters, carboxylic acids)  to alcohols, amides and nitriles to amines.

 

 

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