




The reaction proceeds as follows:
1. \(\text{NaCN}\) reacts with the carbonyl group to form a cyanohydrin (\(\text{-CN}\) and \(\text{-OH}\) groups on the same carbon).
2. Ethanol in the presence of \(\text{H}_2\text{O}^+\) hydrolyzes the cyanohydrin to form a carboxylic acid group (\(\text{-COOH}\)) and retains the hydroxyl group.
Thus, the major products are as shown in option (4), where the carboxylic acid (\(\text{-COOH}\)) and hydroxyl (\(\text{-OH}\)) groups are appropriately positioned.
The correct order of the rate of reaction of the following reactants with nucleophile by \( \mathrm{S_N1} \) mechanism is:
(Given: Structures I and II are rigid) 
| LIST I | LIST II | ||
|---|---|---|---|
| A | Lyman | I | Near IR |
| B | Balmer | II | Far IR |
| C | Paschen | III | Visible |
| D | p-fund | IV | UV |
Which one of the following graphs accurately represents the plot of partial pressure of CS₂ vs its mole fraction in a mixture of acetone and CS₂ at constant temperature?

Hydrocarbons are organic compounds that are entirely made up of only two kinds of atoms – carbon and hydrogen. Typically, hydrocarbons are colourless gases that have very weak odours.
According to experimental evidences, SE (S = substitution; E = electrophilic) reactions are supposed to proceed via the following three steps: