The end product $(C)$ in the following sequence of reactions is:
$HC \equiv CH$ $\xrightarrow[20\% \ H_2SO_4]{1\% \ HgSO_4} A$ $\xrightarrow[H_2O]{CH_3MgX} B$ $\xrightarrow{[O]} (C)$

  • A
    acetic acid
  • B
    isopropyl alcohol
  • C
    acetone
  • D
    ethanol

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Similar Questions

Match the example given in Column-$I$ with the name of the reaction in Column-$II$.
Column-$I$ (Example)Column-$II$ (Reaction)
$(A)$ $CH_3COCl + H_2 \xrightarrow{Pd-C/BaSO_4} CH_3CHO$$(1)$ Friedel-Crafts acylation
$(B)$ $C_6H_5CHO \xrightarrow{NaOH} C_6H_5CH_2OH + C_6H_5COONa$$(2)$ $HVZ$ reaction
$(C)$ $C_6H_6 + CH_3COCl \xrightarrow{AlCl_3} C_6H_5COCH_3$$(3)$ Aldol condensation
$(D)$ $R-CH_2COOH \xrightarrow{Br_2/Red P} R-CH(Br)COOH$$(4)$ Cannizzaro's reaction
$(E)$ $CH_3-CN \xrightarrow{SnCl_2/HCl, H_2O/H^+} CH_3-CHO$$(5)$ Rosenmund's reduction
$(F)$ $2CH_3CHO \xrightarrow{NaOH} CH_3-CH=CH-CHO$$(6)$ Stephen's reaction

Cyclohexylamine when treated with nitrous acid yields $(P)$. On treating $(P)$ with $PCC$ results in $(Q)$. When $(Q)$ is heated with dilute $NaOH$,we get $(R)$. The final product $(R)$ is:

Arrange the following compounds in increasing order of their equilibrium constants for hydration:
$(A). CH_3COCH_3, (B). CH_3CHO, (C). ClCH_2COCH_3, (D). HCHO, (E). ClCH_2CHO$

Which among the following aldehydes is most reactive towards nucleophilic addition reactions?

Which of the following reagents is used to distinguish between acetone and acetophenone?

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