Ortho-Nitrophenol is less soluble in water than p– and m– Nitrophenols because:

(1) Melting point of o–Nitrophenol is lower than those of m– and p– isomers

(2) o–Nitrophenol is more volatile in steam than those of m– and p– isomers

(3) o–Nitrophenol shows Intramolecular H–bonding

(4) o–Nitrophenol shows Intermolecular H–bonding

'x' gm of a compound A3B2C5 contains 'y' gm of A atoms

 

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how to represent the possible fischer projections for 2-bromohexane