Answer:
As for your question, I know to forget to put the options, specifically that your question is incomplete.
Explanation:
Although it could help you by telling you that always a reaction that seeks to balance the pH, and achieve neutrality ... It is necessary to achieve a concentration of OH equal to that of H +, in this way the hydroxyl and the protons.
<h2>Heptene formed is -</h2><h2>

</h2>
Explanation:
The two possibilities when the peroxide is not present
+ HBr →
In presence peroxide,
≡
+ HBr →
- When peroxides are present in the reaction mixture, hydrogen bromide adds to the triple bond of heptane with regioselectivity.
- This reaction is opposite to that of Markovnikov's rule which says that when asymmetrical alkene reacts with a protic acid HX, then the hydrogen of an acid is attached to the carbon with more in number of hydrogen substituents, and the halide (X) group is attached to the carbon with more in number of substituents of alkyl.
- One mole of HBr adds to one mole of 1-heptane.
- The structure of heptene formed is -

Answer:
Waxy leaves protect the strangler fig from drying winds and sunlight that it is exposed to high in the canopy. Perhaps the most amazing part of this extraordinary tree is its flower. What we think of as the fruit is really a hollow, flower-bearing structure called a cyconia.