Which of the following statements correctly explains why bromination reactions are more selective than chlorination reactions.
1 answer:
Answer: A bromine radical is more stable than chlorine radical, so it is less reactive and more choosy.
Explanation:
A chlorine atom being more electronegative in nature is able to attract a hydrogen atom more readily towards itself as compared to a bromine atom.
Since bromine is less electronegative in nature so bromine will be more selective as a hydrogen abstracting agent. As a result, bromine radical is more stable in nature than chlorine radical.
Thus, we can conclude that bromine radical is more stable than chlorine radical, so it is less reactive and more choosy.
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If it is saturated compound then we can calculate the double bond equivalent which will be equal to the number of rings in the compound
the double bond equivalent can be calculated using following formula
Where
H = number of Hydrogen atoms
C = number of carbon atoms
X= number of halogen atoms
N = number of nitrogen atoms
DBE = (10 + 1 - 16 / 2 ) = 3
Hence there are three rings in the compound
The classification of the alcohols gives;
- Compound 1 - Primary alcohol
- Compound 2 - Tertiary alcohol
- Compound 3 - Secondary alcohol
- Compound 4 - Secondary alcohol
Organic compounds occurs in families. The family of compounds is called a homologous series. The homologous series always have a functional group. The functional group is the atom, group of atoms or bond that is responsible for the chemical reactivity of the members of a given homologous series.
Now we know that the alcohols are those organic compounds that contains the -OH group. The could be aliphatic or alicyclic compounds. We shall now proceed to name the kind of alcohols that each of the compounds shown are;
- Compound 1 - Primary alcohol
- Compound 2 - Tertiary alcohol
- Compound 3 - Secondary alcohol
- Compound 4 - Secondary alcohol
Learn ore about alcohols:brainly.com/question/4698220
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