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Explain Hammonds postulate
Because the transition states of the two reactions should resemble the respective carbocation intermediates (Hammond's postulate), study the structures of the two carbocations and verify which should be more stable.
(a) Assign a reason for each of the following statements: (i) Alkylamines are stronger bases than arylamines. (ii) Acetonitrile Is preferred as solvent for carrying out sever
#most wanted question..
Which of the following set of quantum numbers is correct for the 19th electron of chromium: n l m s (a) 3 0
State the function along with one example each of: (i) Antihistamines (ii) Antioxidants (b) What are hybrid propellants?
what is the working principle of potentiometry
Applications of hyperconjugation (A) Carbon-carbon double bond size in alkenes: As we know previously that the more is the number of resonating structures, the very much will
Antiaromaticity - Hydrocarbon Planar cyclic conjugated substances, less stable as compared to the relating acyclic unsaturated species are known as antiaromatic. Molecular orbi
Millon test - Test of proteins Millon's test : while millon's reagent (mercurous & mercuric nitrate in nitric acid) is added to a protein solution, a white precipitate that tur
Polyfunctional Organic Compounds Organic elements that have two or more functional groups are known polyfunctional compounds. Their IUPAC names are acquired as follows, 1. P
There is no difference between a2p and a 3p orbital regarding: (1) Shape (2)Size (3)Energy (4) Value of Ans: Shape
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