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Chemical Properties of Aromatic Nitro Compounds - Electrophilic substitution
Because - NO2 group is deactivating and m-directing, electrophilic substitution (halogenation, nitration and sulphonation) in simple aromatic nitro compounds (for example nitrobenzene) is extremely difficult as compared to that in benzene. Therefore vigorous reaction conditions are utilized for such reaction and the new group enters the m-position.
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Calculate the free energy change of following reaction at298 kelvin H2+I2=2HI if the enthalpy change is 51.8816kj and the entropy change is 166.15j is this reaction thermodyanamica
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Why a covalent bond is directional? The covalent bond is formed as a result of pairing of two electrons in the atomic orbitals of two atoms. The bond then should lie along the
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A useful model of interfacial mass transport makes three assumptions: (i) there is a difference between the concentrations of A at the interface, C A denoted C A in Phases I
Interactive periodic table In this interactive periodic table animation you can view details of all components through clicking on it. You can select the colored through option
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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 solut
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