An organic compound X on treatment with acidified K2Cr2O7 gives a compound Y which reacts with I2 and Na2CO3 to form triiodomethane. The compound X is:
A
CH3OH
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B
CH3COCH3
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C
CH3CHO
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D
CH3CH(OH)CH3
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Solution
The correct option is DCH3CH(OH)CH3 The compound Y should be a ketone as it is responding to iodoform test. Since it is formed by treating X with potassium dichromate(acidic) X should be a secondary alcohol. X is CH3CH(OH)CH3.