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Clickers!. Select the major monosubstitution product:. Either ortho or para to the stronger activating group!. Clickers!. Select the major monosubstitution product:. Select correct reagents. REACTION 1REACTION 2 A: KCN, EtOHHNO 3 B: NaNO 2 , HClCuCN C: NaNO 3 , HClCuCN

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Clickers

Clickers!

Select the major monosubstitution product:


Clickers1

Either ortho or para to the stronger activating group!

Clickers!

Select the major monosubstitution product:


Select correct reagents

Select correct reagents

REACTION 1REACTION 2

A:KCN, EtOHHNO3

B:NaNO2, HClCuCN

C:NaNO3, HClCuCN

D:NaCNNaNO2, HCl

E:NaNO2NaCN, HCl


Select correct reagents1

Select correct reagents

REACTION 1REACTION 2

A:KCN, EtOHHNO3

B:NaNO2, HClCuCN

C:NaNO3, HClCuCN

D:NaCNNaNO2, HCl

E:NaNO2NaCN, HCl


Consider this reaction

Consider this reaction:

The first step in the reaction mechanism is:

A:Deprotonation of the alcohol.

B:Protonation of the methoxyl oxygen.

C:Protonation of the aryl ring.

D:Protonation of the hydroxyl oxygen.


Consider this reaction1

Consider this reaction:

The first step in the reaction mechanism is:

D:Protonation of the hydroxyl oxygen.


Consider this reaction2

Consider this reaction:

The next step in the reaction mechanism is:

A:Protonation of the alkene.

B:Loss of H2O to form a carbocation.

C:1,2-Hydride shift.

D:Proton transfer to the methoxyl group.


Consider this reaction3

Consider this reaction:

The next step in the reaction mechanism is:

B:Loss of H2O to form a carbocation.


And finally

And finally…

But you all knew that anyhow, right?


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