Propose a mechanism, using curved arrows, for the base-catalysed aldol reaction and the subsequent dehydration between furfural and cyclohexanone Q6. КОН H

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Solve Q 4,5,6 with expalanation 

Q6.
Propose a mechanism, using curved arrows, for the base-catalysed aldol reaction
and the subsequent dehydration between furfural and cyclohexanone
КОН
H
Transcribed Image Text:Q6. Propose a mechanism, using curved arrows, for the base-catalysed aldol reaction and the subsequent dehydration between furfural and cyclohexanone КОН H
Part 1 Predict which side of the equilibria, for the following two reactions, lies towards the
left or towards the right and briefly explain why. (Note: You will need to find the pka values
in water of the acid and the conjugate acid to begin to solve the problem).
Q4.
Part 2 Also, show the movement of electrons using curly arrows between the two reactants
of each of the reactions.
?
Reaction 1
H,NEt
H,NEt
H.
H3C
Ethylamine
H3C
:0:
: Он
Reaction 2
CH3
CH3
CH3
CH3
H3C
H3C
Acetone
Q5.
Treatment of a carboxylic acid with trifluoroacetic anhydride leads to an
unsymmetrical anhydride that rapidly reacts with an alcohol to give an ester.
F3C
CF3
trifluoroacetic anhydride
CH;CH,OH
H3C"
+ CF;CO,H
OH
H3C
CF3
H3C
OCH2CH3
Unsymmetrical anhydride 1
Ethyl ester 2
(a) Propose a mechanism, using curved arrows, for the formation of the unsymmetrical
anhydride 1.
(b) Propose a mechanism, using curved arrows, for the formation of the ethyl ester 2.
(c) Why is the unsymmetrical anhydride unusually reactive?
Transcribed Image Text:Part 1 Predict which side of the equilibria, for the following two reactions, lies towards the left or towards the right and briefly explain why. (Note: You will need to find the pka values in water of the acid and the conjugate acid to begin to solve the problem). Q4. Part 2 Also, show the movement of electrons using curly arrows between the two reactants of each of the reactions. ? Reaction 1 H,NEt H,NEt H. H3C Ethylamine H3C :0: : Он Reaction 2 CH3 CH3 CH3 CH3 H3C H3C Acetone Q5. Treatment of a carboxylic acid with trifluoroacetic anhydride leads to an unsymmetrical anhydride that rapidly reacts with an alcohol to give an ester. F3C CF3 trifluoroacetic anhydride CH;CH,OH H3C" + CF;CO,H OH H3C CF3 H3C OCH2CH3 Unsymmetrical anhydride 1 Ethyl ester 2 (a) Propose a mechanism, using curved arrows, for the formation of the unsymmetrical anhydride 1. (b) Propose a mechanism, using curved arrows, for the formation of the ethyl ester 2. (c) Why is the unsymmetrical anhydride unusually reactive?
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