- ✓$CaC{l_2}$
- B$KCl$
- CGlucose
- DUrea
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$\begin{array}{*{20}{c}}
{C{H_3} - CH - CH - C{H_3}\xleftarrow[{ether}]{{Na}}R\,' - Br\,\xrightarrow{{Mg}}'D'\,\xrightarrow{{{H_2}O}}E} \\
{\,\,\,\,|\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,} \\
{\,\,\,\,\,C{H_3}\,\,\,\,\,C{H_3}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}
\end{array}$
(Given: specific rotations of ($+$)-sucrose, ($+$)-maltose, $L$-($-$)-glucose anc. $+(+)$-fructose in aqueous solution are $+66^{\circ},+140^{\circ},-52^{\circ}$ and $+92^{\circ}$, respectively)
($A$) 'invert sugar' is prepared by acid catalyzed hydrolysis of maltose
($B$) . 'invert sugar' is an equimolar mixture of $D$-($+$)-glucose and $D$-($-$)-fructose
($C$) specific rotation of 'invert sugar' is $-20^{\circ}$
($D$) on reaction with $\mathrm{Br}_2$ water, 'invert sugar' forms saccharic acid as one of the products