Basic Mechanistic Steps Flashcards

1
Q

What are the names of the four basic mechanistic steps?

A
  1. Attack of the nucleophile (Make a bond)
  2. Add a proton
  3. Remove a proton
  4. Departure of the leaving group (Break a bond)
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2
Q

What is the “attack of the nucleophile”?

A

It happens when the nucleophile makes a bond with the electrophile.

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3
Q

What is “add a proton”?

A

It happens when the carbon based molecule takes a proton from the non-carbon based molecule

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4
Q

What is “Removing a proton”?

A

It happens when the carbon based molecule gives a proton to the non-carbon based molecule

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5
Q

What is departure of the leaving group?

A

It’s where the most electronegative part of the carbon based atom breaks off

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6
Q

What is the Markovnikov rule?

A

The hydrogen of the electrophile adds to the carbon that has the maximum # of hydrogen.

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7
Q

What is regioselectivity?

A

Regioselectivity determines the CONSTITUTIONAL isomer that is formed (If you select one over the other the reaction is regioselective)

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8
Q

What is a stereoselective reaction?

A

One in which one stereoisomer is formed over the other (It’s optically active)

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9
Q

How are carbocations stabilized?

A

They are stabilized by alkyl groups due to inductive effect and hypercongjugation

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10
Q

What does substituted mean?

A

The most substituted carbon will be the carbon with the most carbons attached

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11
Q

What is the path of electron density through hyperconjugation?

A

Sigma to 2p

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12
Q

Which 1,2 shift is preferred if both are available and equal?

A

1,2 hydrogen shift

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