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But how to solve the second one? When compound C reacts with E?First of all let's identify what C and D are. I assume you got that, but for the sake of clarity, I'll explain it again. For D, we reduced an aldehyde, an ethanal, so we get an alcohol, ethanol. For C, we first reacted C with HCN to get propanenitrile, which upon reacting with sulphuric acid became propanoic acid as hydrolysis via acid of nitriles gives us carboxylic acids. That upon reacting with concentrated sulphuric acid forms prop-2-enoic acid, which is something not part of our course as far as I know, which is why they gave it themselves. Finally, this when reacted with a cold oxidizing agent must form a diol where the double bond exists, which is C. So C must be 2,3-dihydroxy-propanoic acid (I may have gotten the name wrong but you know what I mean): HOCH2CH(OH)COOH
C is: HOCH2CH(OH)COOH
D is: CH3CH2OH
C is a diol and a carboxylic acid, D is an alochol. Obviously when C and D react, the alcohol part of D will react with the carboxylic acid part of C. Thus, the product should be an ester:
HOCH2CH(OH)COOH + HOCH2CH3 = HOCH3CH(OH)COOCH2CH3
Is this correct? Hope I helped.