$P$ and $Q$ are isomers of dicarboxylic acid $C_4H_4O_4$. Both decolorize $Br_2/H_2O$. On heating,$P$ forms a cyclic anhydride.
Upon treatment with dilute alkaline $KMnO_4$,$P$ as well as $Q$ could produce one or more than one from $S$,$T$,and $U$.
$1.$ Compounds formed from $P$ and $Q$ are,respectively:
$(A)$ Optically active $S$ and optically active pair $(T, U)$
$(B)$ Optically inactive $S$ and optically inactive pair $(T, U)$
$(C)$ Optically active pair $(T, U)$ and optically active $S$
$(D)$ Optically inactive pair $(T, U)$ and optically inactive $S$
$2.$ In the following reaction sequences,$V$ and $W$ are respectively:
Give the answer for question $1$ and $2$.

  • A
    $(B, A)$
  • B
    $(B, D)$
  • C
    $(B, C)$
  • D
    $(A, C)$

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Similar Questions

The correct statement$(s)$ about the compound given below is(are):
$A$. The compound is optically active
$B$. The compound possesses centre of symmetry
$C$. The compound possesses plane of symmetry
$D$. The compound possesses axis of symmetry

In the projection formula $[A]$,two groups ($Br$ and $CH_3$) at the chiral center are interchanged to obtain formula $[B]$. When two groups ($C_2H_5$ and $Cl$) of $[A]$ are interchanged,the projection formula $[C]$ is obtained. Which of the following statements is $NOT$ correct for $[A]$,$[B]$,and $[C]$?

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$A$ compound was synthesized by a student,but its structure was not identified. However,his instructor told him that it was a meso compound with $5$ carbons and $2$ stereogenic centers. Which of the following structures should the student consider as possibilities for his compound?

Find out the statements which are not true.
$A$. Resonating structure with more number of covalent bonds and lesser charge separation are more stable.
$B$. In electromeric effect, an unsaturated system shows $+E$ effect with nucleophile and $-E$ effect with electrophile.
$C$. Inductive effect is responsible for high melting point, boiling point and dipole moment of polar compounds.
$D$. The greater the number of alkyl groups attached to the doubly bonded carbon atoms, higher is the heat of hydrogenation.
$E$. Stability of carbanion increases with the increase in $s$-character of the carbon carrying the negative charge.
Choose the correct answer from the options given below.

Which types of isomers of $C_4H_8$ are possible? Give their names and structures.

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