Answer:
Four substitution products are obtained. The carbocation that forms can react with either nucleophile (H2O or CH3OH) from either the top or bottom side of the molecule
Explanation:
An SN1 reaction usually involves the formation of a carbocation in the slow rate determining step. This carbocation is now attacked by a nucleophile in a subsequent fast step to give the desired product.
However, the product is obtained as a racemic mixture because the nucleophile may attack from the top or bottom of the carbocation hence both attacks are equally probable.
The attacking nucleophile in this case may be water or CH3OH
The object has an overall positive charge.
Hydrochloric acid and sodium hydroxide
HCl + NaOh ----> NaCl + H2O
Answer:
Explanation:
It involves the thinking of it as an electrical interaction between the positively charged part of an atom and the negatively charged part as well. Succinctly put, the interaction between the proton of an atom and the electron of an atom.
The relationship between these two sub atomic particles is one of the basis for many chemical bonding, and this is inclusive of all the bonds there exist. Hydrogen, Electrovalent and even Covalent bondings to mention but a few
<span>Li2O2 is the formula
</span>
