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Properties of Bi-phenyl - Hydrocarbon
Bi-phenyl is a colourless solid, melting point 71°C. It goes through usual electrophilic replacement reactions. As aryl set are electron withdrawing, they should comprise deactivating and m-orientating effect. Although, it has been generally given that presence of one benzene ring activates the other for electrophilic substitution and directs the incoming group to o- and p- positions. It has been specified that monosubstitution in the bi-phenyl results in the formation of para isomer like the main product.
Another unique feature of the biphenyl is the behaviour in the direction of second substitution in a monosubstituted biphenyl. The second replacement invariably includes the unsubstituted ring in the ortho and para position no matter what is the nature of substituent previously present.
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Isomers, which vary in the orientation of groups around the double bounded carbon atoms, are known as geometrical Isomers. It is also known as Cis-Trans Isomerism.
maximum no of unpaired electrons a)mn2+ b)ti3+ c)v3+ d)fe2+
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