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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.
why is the valence electron 4s2 in the elelment Sc21 and not 3d1?
If the value of azimuthal quantum number is 3, the possible values of magnetic quantum number would be: (1) 0, 1, 2, 3 (2) 0, - 1, - 2, - 3 (3) 0 ± 1± 2,± 3
Q. Explain about Thiosulphuric Acid? Thiosulphuric acid, H 2 S 2 0 3 , has never been isolated but its salts are well known which contain the thiosulphate ion, S 2 O 2- 3 . Th
how can you explain the fact that lanthinides are highly electopositive?
Barg
how many type of atom?
industrial application of cyanohydrin.?
what is eld
Critical Angle: The particular angle of incidence at which angle of refraction becomes 90 is known as critical Angle and it is denoted by θc
what points should be included in an assignment on van der waals forces
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