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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.
By the action of CO on methyl alcohol Methyl alcohol and carbon monoxide react together under a pressure of 30 atmospheres and 200°C in presence of a catalyst cobalt octacarbon
Mesomeric forms are the possible locations of electrons at a single instant, if you get what I mean. Like, an adjacent double and single bond in a molecule. The resonance form, how
It looks at how the ionic product varies with temperature, and how that ... page, we shall calculate the concentration of hydroxonium ions present in pure water. Kw is called
Q. Explain Collision Theory? Ans. Why do some reactions take place faster than others? What actually happens in a chemical reaction? Consider a gaseous reaction of the typ
After the treatment of A with concentrated H 2 SO 4 and acetonitrile under thermodynamic conditions, only E formed that was subsequently hydrolyzed to B. Draw the structure of
In nitromethane N-O bondlength is 1.21A° while normal N-O bondlength is 1.36 A° and for N=O it is 1.18A°..Explain why
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The enthalpy change (ΔH) in a reaction is equal to the heat input under conditions of constant pressure and temperature. It is not equal to the total energy change, as work may be
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