The following carbocation undergoes a rearrangement by a hydride shift + The rearrangement converts a secondary into a t

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The following carbocation undergoes a rearrangement by a hydride shift + The rearrangement converts a secondary into a t

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The Following Carbocation Undergoes A Rearrangement By A Hydride Shift The Rearrangement Converts A Secondary Into A T 1
The Following Carbocation Undergoes A Rearrangement By A Hydride Shift The Rearrangement Converts A Secondary Into A T 1 (25.71 KiB) Viewed 16 times
The Following Carbocation Undergoes A Rearrangement By A Hydride Shift The Rearrangement Converts A Secondary Into A T 2
The Following Carbocation Undergoes A Rearrangement By A Hydride Shift The Rearrangement Converts A Secondary Into A T 2 (14.98 KiB) Viewed 16 times
The following carbocation undergoes a rearrangement by a hydride shift + The rearrangement converts a secondary into a tertiary carbocation The rearranged carbocation is more stable because of resonance Hydride shifts are always favorable The carbocation after rearrangement is more stable because it is further from t

LUIT undergoes a rearrangement by a hydride shift as shown below The reason why The rearrangement converts a secondary into a tertiary carbocation The rearranged carbocation is more stable because of resonance Hydride shifts are always favorable The carbocation after rearrangement is more stable because it is further from the end of the molecule
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