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Arrange benzene, n-hexane and ethyne in decreasing order of acidic behavior. Also give reason for this behavior?

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Since s-electrons arc closer to the nucleus, therefore as the s-character of the orbital making the C-H bond increases the electrons of C-H bond lies closer and closer to the carbon atom. In other words, the partial +ve charge on the H-atom and hence the acidic character increases as the s-character of the orbital increases. Thus, the acidic character decreases in the order 

Ethyne > Benzene > Hexane

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