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Tardigrade
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Chemistry
In keto-enol tautomerism of dicarbonyl compounds the enol-form is preferred in contrast to the keto-form, this is due to
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Q. In keto-enol tautomerism of dicarbonyl compounds the enol-form is preferred in contrast to the keto-form, this is due to
VITEEE
VITEEE 2015
A
presence of carbonyl group on each side of $ - CH_2 - $ group
0%
B
resonance stabilisation of enol form
82%
C
presence of methylene group
18%
D
rapid chemical exchange
0%
Solution:
Resonance stabilisation of enol form as shown