Step 1: Recall the requirement for hydrogen bonding.& nbsp;
Hydrogen bonding requires:
\[ \boxed{ \text{A hydrogen atom bonded to } \mathrm{O},\ \mathrm{N}\ \text{or}\ \mathrm{F} } \]
along with a lone pair on a nearby electronegative atom.
Step 2: Examine each compound.
\[ \begin{aligned} \text{Salicylaldehyde} & amp;\rightarrow \text{Intramolecular hydrogen bonding present},\\ \text{Catechol} & amp;\rightarrow \text{Hydrogen bonding present},\\ \text{Salicylic acid} & amp;\rightarrow \text{Intramolecular hydrogen bonding present},\\ \text{Acetophenone} & amp;\rightarrow \text{No }-\mathrm{OH}\text{ or }-\mathrm{NH}\text{ group}. \end{aligned} \]
Therefore, acetophenone cannot form hydrogen bonding within its molecule.
Step 3: State the answer.
Hence,
\[ \boxed{\text{Hydrogen bonding does not exist in acetophenone}.} \]
Therefore, the correct option is \[ \boxed{(D)}. \]
| Molisch's lest | Barfoed Test | Biuret Test | |
|---|---|---|---|
| A | Positive | Negative | Negativde |
| B | Positive | Positive | Negative |
| C | Negative | Negative | Positive |