Question
In: Chemistry
Imine formation with the reaction of aniline with benzaldehyde. Draw mechanism.
Imine formation with the reaction of aniline with benzaldehyde. Draw mechanism.
Solutions
queen_honey_blossom answered 2 years agoRelated Solutions
Draw the mechanism for the formation of the imine (forward reaction) and the hydrolysis of the imine (reverse reaction.)
Draw the mechanism for the formation of the imine (forward reaction) and the hydrolysis of the imine (reverse reaction.)
Give the detailed mechanism for the formation of an imine:
Give the detailed mechanism for the formation of an imine:
Consider the acid-catalyzed mechanism of the imine formation (provided in the introduction). How would the reverse reaction proceed?
Consider the acid-catalyzed mechanism of the imine formation (provided in the introduction). How would the reverse reaction proceed? Draw out the mechanism and justify the steps.
Consider the acid-catalyzed mechanism of the imine formation (provided in the introduction). How would the reverse reaction proceed?
2. The price of a bond is generally
determined by
a. the relation between the coupon
rate and the current market rate of similar investments
b. the stated interest rate of the
bond
c. how many bonds are issued
d. who buys the bonds
3. How is the consolidated
statements treatment of constructive gain or loss on intercompany
bond investments different from the treatment of unrealized profit
on intercompany sales of inventory?
a. Constructive gain or loss is
deferred until...
Use curved arrows to predict the complete mechanism of formation of the imine shown below.
Use curved arrows to predict the complete mechanism of
formation of the imine shown below.
Draw the mechanism and label products and reactants for the synthesis of aniline to 4-Bromo-2-Chloroacetanilide: Aniline...
Draw the mechanism and label products and reactants for the
synthesis of aniline to 4-Bromo-2-Chloroacetanilide:
Aniline + Acetic Anhydride --> Acetanilide + Acetic Acid
Acetanilide + Bromine --> 4-Bromoacetanilide
STEP 1: Hydrochloric Acid + Sodium Chlorate --> Chlorine +
Water + Sodium Chloride
STEP 2: 4-Bromoacetanilide + Chlorine -->
4-Bromo-2-Chloroacetanilide
4-Bromo-2-Chloroacetanilide + Ethanol -->
4-Bromo-2-Chloroaniline + Ethyl Acetate
Show all lone pairs or formal charges.
Show an extraction scheme in how to purify the benzaldehyde. Draw the mechanism for each of...
Show an extraction scheme in how to purify the benzaldehyde.
Draw the mechanism for each of the four products that can be formed
in the first part of the reaction.
a) Draw the mechanism for nitration of methyl benzoate. Include formation of the electrophile. The mechanism...
a) Draw the mechanism for nitration of methyl benzoate. Include
formation of the electrophile. The mechanism should explain why the
meta product is obtained.
b) Why is the nitration of aromatic rings a useful reaction?
In the reaction mechanism of chymotrypsies, formation of the tetrahedral intermediate is then followed by the...
In
the reaction mechanism of chymotrypsies, formation of the
tetrahedral intermediate is then followed by the formation of an
acyl enzyme Intermediate. What active site residue(s) /are
responsible for forming the first intermediate , and what type of
catalysis occurring the first step of the reaction ?
Draw the mechanism for the formation of the carbocation obtained. Explain why the solution of this...
Draw the mechanism for the formation of the carbocation
obtained. Explain why the solution of this carbocation is colored.
See below for information on the experiment:
To test for a carbocation in a lab, we did the following:
1) Dissolve a small amount of diphenylmethanol into methanol,
and add concentrated sulfuric acid dropwise. This caused the
solution to turn yellow/orange.
2) Dissolve a small amount of benzophenone into methanol, and
add concentrated sulfuric acid dropwise. The solution remained
clear.
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