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In CH3CH2OH, the bond that undergoes heterolytic cleavage most readily is
- a)C—C
- b)C—O
- c)C—H
- d)O—H
Correct answer is option 'D'. Can you explain this answer?
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Most Upvoted Answer
In CH3CH2OH, the bond that undergoes heterolytic cleavage most readily...
Due to high difference in electronegativity, polarity of the bond is high. So it's easier to break C—O bond.
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In CH3CH2OH, the bond that undergoes heterolytic cleavage most readily...
NOTE : Heterolytic fission occurs when the two atoms differ considerably in their electronegativities.
O – H bond undergoes cleavage most readily because O and H differ markedly in their electronegativity and further oxygen being highly electronegative can accommodate the negative charge more effectively developed after the cleavage.
O – H bond undergoes cleavage most readily because O and H differ markedly in their electronegativity and further oxygen being highly electronegative can accommodate the negative charge more effectively developed after the cleavage.
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In CH3CH2OH, the bond that undergoes heterolytic cleavage most readily isa)C—Cb)C—Oc)C—Hd)O—HCorrect answer is option 'D'. Can you explain this answer?
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