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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.
Construction and working of calomel electrode with a labelled diagram
Steam supply for experiments in heat A tin with a press-on lid may be used to make a steam can. Punch two holes in the lid and solder by them one long and one short pip
When an electron jumps from L to K shell: (1) Energy is absorbed (2) Energy is released (3) Energy is sometimes absorbed and sometimes released (4) Energy is nei
what does ammonia gas and chloride mixed, make?
The first use of quantum theory to explain the structure of atom was made by: (1) Heisenberg (2 )Bohr (3) Planck (4) Einstein Ans: Bohr
outline the structure of the isomeric alkyl halides with molecular formula c4h9cl
why do soap not work in hard water ?
complete reaction
dithiazone.
sn1 and sn2 reactions
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