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for reducing carbonyls (aldehydes, ketones, acids) into alcohols. Halogenating Agents cap P cap C l sub 3 cap P cap C l sub 5 cap S cap O cap C l sub 2 reactions and reagents op agarwal pdf exclusive

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C–C bond formation

, such as organometallics or oxidants, for a deeper technical breakdown? Alcohols: TBS/TBDMS (stable to base, removable with TBAF),

Alcohols: TBS/TBDMS (stable to base, removable with TBAF), MOM (acid-labile), benzyl (hydrogenolysis).

Amines: Boc (acid-labile), Fmoc (base-labile).

Carbonyls: Acetals/ketals for aldehyde/ketone protection (acidic deprotection).

Tip: Plan orthogonal protections to allow selective deprotection later.

The exam hall was silent, save for the scratching of pens. Aryan flipped to the Chemistry section. His heart skipped a beat. Question 42 was a convoluted mess involving a Grignard reagent reacting with a nitrile in acidic conditions.