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how to find stability of carbocations in benzene ring..??? and how how to find optically inactive isomers ??? (say of--C2H5Cl) how to find the weakest C-X (carbon-halogen bond in a benzene ring????
If an electron has spin quantum number of +1/2 and a magnetic quantum number of -1 , it cannot be presented in an: (1) d -orbital (2) f -orbital (3) p -orbital (4)s-
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Melting and freezing points: When a pure solid substance is heated through its melting point (melting temperature), the solid changes to a liquid. At the melting point equilibr
The hydration of propene The hydration of propene includes the usual mechanistic steps of alkene protonation to form a carbocation followed by the nucleophilic reaction of wate
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unit of ell constant .
basically 3 degree carbocations are more stable as compared to 2 degree and one degree. for optically inactive isomer look for terms like racemic mixture and diastomers and the weakest halgon bond depends on leaving group halogen better leaving group weaker the bond is
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