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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.
1. The temperature of the warm water bath is recorded too high. How will this technique error affect the reported activation energy for the reaction - too high or too low? explain
clark''s method
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Which of the following is not isoelectronic : (1) Na + (2) Mg 2+ (3) O 2- (4) Cl - Ans:(d)Cl -
Explain bond dipole for dimethylmagnesium The bond dipole for dimethylmagnesium should show that C is at the negative end of the C-Mg bond, because carbon is more electronegati
Q. Determine the Uniqueness of Carbon? Ans. Carbon forms a very large number of compounds--over 4,000,000. This is far more than the number of compounds of all other eleme
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Explain the Effects of Temperature on multicomponent systems? For some of the derivations in this chapter, we will need an expression for the rate at which the ratio μ i /T var
what is dipole moment?
what is rayon?what are the things made of it?
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