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Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is:

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Important Questions on Aldehydes, Ketones and Carboxylic Acids

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The order of reactivity of phenyl magnesium bromide (PhMgBr) with the following compounds:

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Acetone is treated with excess of ethanol in the presence of hydrochloric acid. The product obtained is:
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Which one is most reactive towards Nucleophilic addition reaction? 
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Reaction of a carbonyl compound with one of the following reagents involves nucleophilic addition followed by elimination of water. The reagent is _____.

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Which one of the following esters gets hydrolysed most easily under alkaline conditions? 
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Which of the following reagents would distinguish cis-cyclopenta-1,2- diol from the trans-isomer?