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Free radical aromatic substitution - Hydrocarbon
The aromatic substitution reactions that follow free radical mechanisms are extremely few and have limited synthetic value. Although some typical illustartions of these reactions are:
The method of chlorination of benzene at high temperature is identical to that of the free radical aliphatic substitution
Cl2 → Cl + Cl (Chain initiation)
C6H6 + Cl → C6H5+HCl (H- abstraction)
C6H5 + Cl2 → C6H5Cl + Cl (Chain propagation)
The bond energy of an O- H bond is 109 kcal mol 1. When a mole of water is formed from H and O atoms, then 218 kcal is released. Two O-H bonds are there is H2O so 2*109 kcal an
electrophilic substitution reactions and mechanisms
Write the electron configuration for Tl why do we use F block and how do i count the subshells in that case?
glutamic acid standard estimation protocol
how to report phase change
The valence electron in the carbon atom are: (1) 0 (2) 2 (3) 4 (4) 6 Ans: 4
explain the mechanism
The determination of k is not a strait forward exercise. Model it from first principles using Bernoulli's equation would produce a square root relationship and would probably have
s block
Branched chain polymers - Classification of polymers These are polymers where the monomers are connected to make long chains with side chains or branches of dissimilar sizes.
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