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In cis isomer, bulky methyl groups are close by and have steric repulsion, so they are less stable. But in trans, methyl groups being on opposite side are far away from each other so that there is no steric repulsion and hence more stable.



In 2,6-di(t-butyl) benzoic acid, since there is steric hindrance to the stabilization of carboxylate ion through solvation, it is less acidic than benzoic acid.

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SN2 reactivity of tertiary halides is least because of steric hindrance.
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Steric hindrance to the approach of alcohol to the reaction site on carboxylic acid will lower the rate of esterification.


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