pptx, 2.41 MB
pptx, 2.41 MB
docx, 45.55 KB
docx, 45.55 KB

This lesson allows the students to see that ALL electrophilic substitution reactions of benzene progress by the same mechanism: 1 - formation of the electrophile in situ; 2 - attack of the electrophile on the ring; 3 - reformation of the catalyst.

6.1.1 (d) The electrophilic substitution of aromatic compounds with:

(i) concentrated nitric acid in the presence of concentrated sulfuric acid

(ii) a halogen in the presence of a halogen carrier

Creative Commons "Sharealike"

Reviews

Something went wrong, please try again later.

This resource hasn't been reviewed yet

To ensure quality for our reviews, only customers who have downloaded this resource can review it

Report this resourceto let us know if it violates our terms and conditions.
Our customer service team will review your report and will be in touch.