Explain carbocation intermediate, Chemistry

Assignment Help:

Explain carbocation intermediate

When 3-methyl-1-butene undergoes acid-catalyzed hydration, rearrangement happens because carbocation intermediates are included. (See the solution) Oxymercuration-reduction gives addition without rearrangement because the intermediate is a cyclic mercurinium ion, which does not rearrange.

 

1531_chemsitry.png


Related Discussions:- Explain carbocation intermediate

Stoichiometry and Mole Concept, What volume of oxygen would be required to ...

What volume of oxygen would be required to burn completely 200 ml of acetylene and what would be the volume of carbon dioxide formed?

What is the basicity of h3po4?, The Basicity is 3 as there are 3 H atoms th...

The Basicity is 3 as there are 3 H atoms that can be displaced from compound.

The fermi level is, The Fermi level is The highest occupied energy lev...

The Fermi level is The highest occupied energy level at 0 0 K.

F-block elements, electronic cofiguration of f-block elements

electronic cofiguration of f-block elements

Transitions between energy levels, A red flame is produced when LiCl is hea...

A red flame is produced when LiCl is heated. How can I determine which transition between the energy levels produces this colour?

Write Your Message!

Captcha
Free Assignment Quote

Assured A++ Grade

Get guaranteed satisfaction & time on delivery in every assignment order you paid with us! We ensure premium quality solution document along with free turntin report!

All rights reserved! Copyrights ©2019-2020 ExpertsMind IT Educational Pvt Ltd