The +I Effect & Bond Breakage in Alcohols & Acids

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The +I effect of alkyl groups in alcohols increases the negative charge on the oxygen atom, facilitating the breakage of the C-O bond. Conversely, in carboxylic acids, the +I effect decreases the positive charge on the carbon atom, making the breakage of the C=O bond more difficult. This effect promotes an electron-withdrawing influence on the hydroxyl oxygen, aiding in proton release. The resulting carboxylate anion is stabilized through resonance hybrid structures. Understanding these dynamics is crucial for grasping bond behavior in organic compounds.
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In alcohols, the negative charge on 'Oxygen atom' increases due to '+I effect' of alkyl groups. While in acids, the '+I effect' of alkyl groups decreases the positive charge on the 'Carbon atom'.

In the first case the +I effect makes it easier to break the C-O bond while in the second case the +I effect makes the breakage of 'C=O' bond difficult. Please explain.
 
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In terms of the second case with the carboxyl group: The + charge about the carbon
promotes an electron withdrawing effect on the hydroxyl oxygen by induction. This facilitates release of the proton.
The carboxylate anion is then stablized as a two structure resonance hybrid.

=O
C
-O-


-O-
C
=O

note: scroll down to the Chemistry section as this type of question is better there
 
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