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Answer:
Photosynthetic cell
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Answer: option a and d
Explanation:
Option A- Benzene undergoes substitution reaction
Example : benzene reacts with chlorine to form chlorobenzene, in the presence of Iron
(iii) chloride as a catalyst
C6H6 + Cl2 ---> C6H5Cl + HCl
Option D- Benzene also undergoes addition reaction
Example: benzene reacts with hydrogen , in the presence of nickel as a catalyst to form
cyclohexane
C6H6 + 3H2 ---> C6H12
Reasons why Option B isn't the answer
Although benzeme has degree of unsaturation but it's not five degree of unsaturation.
Benzene has 6 carbon atoms and 4 degrees of unsaturation (1 ring and 3 double
bonds).
If you work backwards and double the degrees of unsaturation you have 8 degrees of
unsaturation instead of 5.
Option C - Benzene isn't a saturated hydrocarbon
A free-radical substitution reaction is likely to be responsible for the observations. The reaction mechanism of a reaction like this can be grouped into three phases:
- Initiation; the "light" on the mixture deliver sufficient amount of energy such that the halogen molecules undergo homologous fission. It typically takes ultraviolet radiation to initiate fissions of the bonds.
- Propagation; free radicals react with molecules to produce new free radicals and molecules.
- Termination; two free radicals combine and form covalent bonds to produce stable molecules. Note that it is possible for two carbon-containing free-radicals to combine, leading to the production of trace amounts of long carbon chains in the product.
Initiation

where the big black dot indicates unpaired electrons attached to the atom.
Propagation






Termination

1) acid
2) ether
3) ester
4) aldehyde
5) ketone
6) amine
7) alcohol
2 is right am 70 percent sure