Arrange ethanal , propanal, propanone, butanone in increasing order of their reactivity in nucleophilic addition reactions
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Butanone < propanone < propanal < ethanal
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as we move from ethanal → propanal → propanone → butanone, the +I effect of alkyl group increases and hence +ve charge on carbonyl carbon progressively decreases and hence the attack of nucleophile becomes slower and slower. also stearic hindrances due to alkyl groups increase.
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