MBB 222 Lecture Notes - Lecture 19: Electrophile, Nucleophile, Enzyme
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What is the first step in the mechanism of an EAS reaction?
The formation of a strong electrophile. | |
Loss of a proton from the arenium ion. | |
The attenuation of the electrophilicity of an electrophile. | |
The diminution of the nucleophilicity of the benzene's Ï-electrons. | |
Loss of a proton from the nucleophile. | |
Arenium ion incontinence. | |
The formation of a strong nucleophile. | |
Benzene's Ï-electrons nucleophilicly attacking an electrophile. |
What is the second step in the mechanism of an EAS reaction?
The attenuation of the electrophilicity of an electrophile. | |
The formation of a strong nucleophile. | |
Benzene's Ï-electrons nucleophilicly attacking an electrophile. | |
Loss of a proton from the arenium ion. | |
The diminution of the nucleophilicity of the benzene's Ï-electrons. | |
Arenium ion incontinence. | |
Loss of a proton from the nucleophile. | |
The formation of a strong electrophile. |
What is the third step in the mechanism of an EAS reaction?
Arenium ion incontinence. | |
The attenuation of the electrophilicity of an electrophile. | |
The diminution of the nucleophilicity of the benzene's Ï-electrons. | |
Loss of a proton from the nucleophile. | |
Benzene's Ï-electrons nucleophilicly attacking an electrophile. | |
Loss of a proton from the arenium ion. | |
The formation of a strong electrophile. | |
The formation of a strong nucleophile. |