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(A) ($o$-Nitrophenol) shows strong intramolecular $H$-bonding due to the proximity of the $-OH$ and $-NO_2$ groups,which prevents intermolecular $H$-b

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$b$ only

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(A) ($o$-Nitrophenol) shows strong intramolecular $H$-bonding due to the proximity of the $-OH$ and $-NO_2$ groups,which prevents intermolecular $H$-bonding.$b$ ($N$-($4$-hydroxyphenyl)acetamide) contains both $-OH$ and $-NH-$ groups,which are capable of forming significant intermolecular $H$-bonding with other molecules.$c$ ($2,6$-di-tert-butylphenol) has two bulky tert-butyl groups at the ortho positions,which create significant steric hindrance around the $-OH$ group,preventing it from participating in intermolecular $H$-bonding.Therefore,only compound $b$ shows significant intermolecular $H$-bonding.

The compound/s which will show significant intermolecular $H$-bonding is/are :
$(a)$ $o$-Nitrophenol
$(b)$ $N$-($4$-hydroxyphenyl)acetamide
$(c)$ $2,6$-di-tert-butylphenol

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The compound/s which will show significant intermolecular $H$-bonding is/are : $(a)$ $o$-Nitrophenol$(b)$ $N$-($4$-hydroxyphenyl)acetamide$(c)$ $2,6$-di-tert-butylphenol