Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive. Since soft nucleophiles are less strongly solvated than hard nucleophiles, these solvents boost the relative reactivity of soft anions.
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Ethanol is either a nucleophile or a base.</h3>
The ethanol is a base Because carbocation is an extremely reactive species, a base or nucleophile as weak as ethanol can replace or remove it. SN1 and E1 would not be conceivable without the carbocation or a strong departing group.
<h3>How do solvents impact anionic nucleophile's reactivity?</h3>
In polar aprotic solvents, nucleophilic substitution reactions of anionic nucleophiles often proceed more quickly. The normal relative reactivity order in such solvents (like DMSO)is Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive.
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K gives 1 electron, and Br takes 1 electron.
<span>Heavy metals like mercury enter waterways by industrial dumping and poor regulatioin of effluent, and they also enter soil through a similar manner, in which waste is disposed of imporperly. Another source of heavy metals are the gases leaving industry carrying these metals. The metals fall as a solid on to soil and water ways. Therefore, the answer is D.</span>
The highlighted atoms have sp2 - sp3 hybridization. The highlighted atoms are carbon and nitrogen as shown.
The structure of Xanthine is shown in the image attached to this answer. The indicated atoms are Carbon and nitrogen as shown. Let us remember that hybridization has to do with the mixing of atomic orbitals to form appropriate hybrid orbitals that are suitable for overlap with orbitals of other atoms.
The highlighted carbon atom is sp2 hybridized because it has a carbon nitrogen double bond while the highlighted nitrogen atom is sp3 hybridized. Therefore, the highlighted atoms have sp2 - sp3 hybridization.
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