Write the reactions involved when D-glucose is treated with the following reagents: (a) HCN (b) Br\(_2\) water
(a) Reaction of D-glucose with HCN: When D-glucose is treated with hydrogen cyanide (HCN), it undergoes cyanohydration to form a cyanohydrin, specifically D-glucose cyanohydrin. \[ \text{D-glucose} + HCN \rightarrow \text{D-glucose cyanohydrin} \]
(b) Reaction of D-glucose with Br\(_2\) water: When D-glucose is treated with bromine water, it undergoes oxidation at the aldehyde group. This converts the aldehyde group to a carboxylic acid group, and the product is gluconic acid. \[ \text{D-glucose} + Br_2 \text{(water)} \rightarrow \text{Gluconic acid} \]
(A) Explain the following reactions and write chemical equations involved:
(a) Wolff-Kishner reduction
(b) Etard reaction
(c) Cannizzaro reaction
Consider the following compounds: K$_2$O$_2$, H$_2$O$_2$, and H$_2$SO$_4$
The oxidation states of the underlined elements in them are, respectively:
Write the structures of A, B, and C in the following sequence of reactions:
Analyzing the following reaction, ascertain the final product:
Two batteries of emf's \(3V \& 6V\) and internal resistances 0.2 Ω \(\&\) 0.4 Ω are connected in parallel. This combination is connected to a 4 Ω resistor. Find:
(i) the equivalent emf of the combination
(ii) the equivalent internal resistance of the combination
(iii) the current drawn from the combination