Among the following,the conformation that cor | vedclass

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(B) The most stable conformation of meso-butane-$2,3$-diol is determined by the presence of intramolecular hydrogen bonding between the two hydroxyl $

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(B) The most stable conformation of meso-butane-$2,3$-diol is determined by the presence of intramolecular hydrogen bonding between the two hydroxyl $(-OH)$ groups. In the Newman projection of the meso form,when the two $-OH$ groups are in a gauche position relative to each other,they can form an intramolecular hydrogen bond,which stabilizes the conformation. Comparing the given options,the structure that shows the $-OH$ groups in a gauche orientation allowing for this stabilization is represented in option $B$.

Among the following,the conformation that corresponds to the most stable conformation of meso-butane-$2,3$-diol is -

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