Answer:
hydration reaction
Explanation:
The type of reaction would be hydration reaction.
<u>Hydration reaction generally involves a chemical reaction of water with another reactant and in which the water ends up being converted to another product entirely. </u>
A good example of hydration reaction is the reaction between alkene and water leading to the production of alcohol.
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The important thing to note is the reason why electron react is due to the instability of the electrons. All elements wants to aim the electron configuration of the noble gases. This is the most stable form in which each of the orbitals are sufficiently filled. When it comes to bonding, the order of reactivity is: alkynes > alkenes > alkanes. Alkynes are compounds with triple bonds, alkenes with double bonds and alkanes with single bonds. The single bonds are called saturated hydrocarbons. This is because they have reached stability, so it is quite difficult to react this with reducing or oxidizing agents. Alkynes and alkenes are unsaturated hydrocarbons. They readily react with reducing and oxidizing agents so as to become saturated, as well. The underlying principle for this is that single bonds contain sigma bonds which is the head-on overlapping of electrons. These is the strongest type of covalent bond. Double and triple bonds contain pi bonds which is the side overlapping of electrons orbitals. Hence, these electrons would be easily separated making it more reactive especially during protonation.
Answer: The law of corresponding states is an empirical law according to which the equations of states for real gases are similar when these gases are expressed in reduced temperature, pressures, and volumes at critical point.
Answer:
see explaination
Explanation:
We are given the (R)-3-bromo-2,3-dimethylpentane and asking to draw the curved arrow which is the showing the mechanism for first-order substitution and first-order elimination reactions. We know the formation of carbocation is the rate determining step in the first-order substitution and first-order elimination reactions.
So in the (R)-3-bromo-2,3-dimethylpentane there is –Br gets removed and formed the tertiary carbocation which is more stable, so the curved arrows in Box 1 to depict the flow of electrons and intermediate in Box 2.
Check attachment
