Sulfonation | Aromatic Compounds | Organic chemistry | Khan Academy

[@zainabahmad9445]

thank u soooooooo much...u saved my day...😍

[@mr.n_r_maher_9jayveervachh534]

Great explanation sir Thank You

[@johnmandrake8829]

great explanation. Good job!

[@arvindkumarm1927]

In the above rxn which is the rate determining step??? In sulphonation of benzene Also in iodination??

[@arvindkumarm1927]

In iodination of benzene, deutrobenzene(C6D6) nd tritiobenzenzene(C6T6) The rate determining step Is the breaking vof C-H bondCan u pls explain Y??The same happens in sulphonation of benzene

[@saurabhinorange]

Can you also do side chain oxidation using kmno4 Thanks

[@zabign7249]

is it possible to do a friedel craft after sulfonation

[@goldenfriedc]

the so3h has one bond between the oxygen and sulfur? that oxygen should have a bond between H and S?

[@pieter-ruannpieters9250]

why would the H2O take another H from the benzene, rather than the H going to the (HSO4)- from the previous steps?

[@lelo379]

H2SO4 is a strong acid, therefore the reaction HSO4- + H+ -> H2SO4 is highly discouraged

[@AnshMehtaGR8]

how can a strong acid behave as an base and autoprotonate itself???

[@motivations-d6s]

I was 5 years old

[@AnshMehtaGR8]

why this is a reversible reacn ??? is this due to its Energy Profile??