What is the product of the following reaction?

  • A
    $N$-methylphthalimide
  • B
    $2-$hydroxy$-2-$methyl-isoindoline$-1-$one
  • C
    Phthalhydrazide
  • D
    Indane$-1,3-$dione

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Ester and acetamide are distinguished by

Match the compounds possessing carbonyl carbon in Column-$I$ with their formulas in Column-$II$ and examples in Column-$III$:
Column-$I$ (Name)Column-$II$ (Formula)Column-$III$ (Example)
$(A)$ Ketone$(i)$ $R-CO-OH$$(p)$ $CH_3CHO$
$(B)$ Carboxylic acid$(ii)$ $R-CO-H$$(q)$ $CH_3COOH$
$(C)$ Amide$(iii)$ $R-CO-R'$$(r)$ $CH_3CONH_2$
$(D)$ Aldehyde$(iv)$ $R-CO-NH_2$$(s)$ $CH_3COC_2H_5$

Product $(X)$ is

With reference to the scheme given,which of the given statement$(s)$ about $T$,$U$,$V$ and $W$ is (are) correct?
$A$. $T$ is soluble in hot aqueous $NaOH$
$B$. $U$ is optically active
$C$. Molecular formula of $W$ is $C_{10}H_{18}O_4$
$D$. $V$ gives effervescence on treatment with aqueous $NaHCO_3$

Which $\beta$-keto acid shown will not undergo decarboxylation?

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