(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
$(a)$ Heated : it is charred
$(b)$ $I_2$ solution : no violet colour
$(c)$ Fehling solution : reddish brown ppt. is observed
$(d)$ It does not reduce copper$(II)$ acetate to $Cu_2O$ . No red precipiated is observed in $5/ min$
The carboxylate which satisfy all the above observation