Aldehydes and ketones undergo reduction. The products formed depend on the reducing agent.
CH3−CH=CH−CHOLiAlH4−−−−→(P)
C6H5−CHONa,C2H5OH−−−−−−−−→(Q)
The compounds (P) and (Q) respectively are :
A
CH3−CH2−CH2−CHOandC6H5−CH3
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B
CH3−CH2−CH2−CHOandC6H5−CH2OH
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C
CH3−CH=CH−CH2OHandC6H5−CHOH−CHOH−C6H5
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D
C6H5−CH3 and CH3−CH2−CH2−CH3
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Solution
The correct option is CCH3−CH=CH−CH2OHandC6H5−CHOH−CHOH−C6H5 When the reducing agent is lithium aluminium hydride, the aldehyde group is reduced to primary alcohol but the carbon-carbon double bond is unaffected.
CH3−CH=CH−CHOLiAlH4⟶CH3−CH=CH−CH2OH(P)
When the reducing agent is sodium in ethanol, the aldehyde group is reduced to alcohol and the product formed is obtained by coupling reaction.