The two compounds given below are
enantiomers
identical
optically inactive
diastereomers
$P$ and $Q$ are isomers of dicarboxylic acid $C _4 H _4 O _4$. Both decolorize $Br _2 / H _2 O$. On heating, $P$ forms the 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 $U$.$Image$
$1.$ Compounds formed form $P$ 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 :$Image$
mcq $Image$
Give the answer question $1$ and $2.$
The following pair of compounds is best described as
In the reaction $C{H_3}CHO + HCN \to C{H_3}CH(OH)CN$ a chiral centre is produced. This product would be
Correct configuration of the following molecule is