The intramolecular Aldol condensation of 2,6-heptanedione with base may produces two possible B-hydroxyl ketones as shown in the following reaction pathway. CH, (1) OH CH, (A) 3-Methyl-2-cyclohexenone CH, CH, (2) Он CH, 2,6-Heptanedione (B) Methyl(2-methyl-1-cyclobutenyl)ketone (i) Write detailed mechanisms for both the reactions (1) and (2).

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter23: Carbonyl Condensation Reactions
Section23.3: Dehydration Of Aldol Products: Synthesis Of Enones
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The intramolecular Aldol condensation of 2,6-heptanedione with base may produces two possible
B-hydroxyl ketones as shown in the following reaction pathway.
CH,
(1) OH
CH,
(A) 3-Methyl-2-cyclohexenone
CH,
CH,
(2) Он
CH,
2,6-Heptanedione
(B) Methyl(2-methyl-1-cyclobutenyl)ketone
(i)
Write detailed mechanisms for both the reactions (1) and (2).
Transcribed Image Text:The intramolecular Aldol condensation of 2,6-heptanedione with base may produces two possible B-hydroxyl ketones as shown in the following reaction pathway. CH, (1) OH CH, (A) 3-Methyl-2-cyclohexenone CH, CH, (2) Он CH, 2,6-Heptanedione (B) Methyl(2-methyl-1-cyclobutenyl)ketone (i) Write detailed mechanisms for both the reactions (1) and (2).
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