Answer:
To synthesize cis-2-methylcyclopentyl from methycyclopentanol, you need to replace the acetate hydroxyl group with acetate by inverting the configuration.
Explanation:
To understand the process, you need to understand the nucleophilic mechanism taking place in the process. This is the first stage of the process. Hydroxide is a poor leaving group, to it must be converted to a good leaving group. To effect the change, it is necessary to use p-toluenesuphate.
p-toluenesuphate is favored because this can be prepared by a reaction that alters none of the bonds attached to the stereogenic center.
The reaction of p-toluensulfonate with potassium acetate in acetic acid effects the conversion to give the final product: cis-2-methylcyclopentyl.
Cd2+ + 2Hg Cd + Hg22+. Both Cd2+ + 2e Cd(s) -0.40 and Hg22+ + 2e 2Hg(l) 0.79
A chemical reaction known as an oxidation-reduction (redox) reaction includes the exchange of electrons between two substances.
Any chemical reaction in which the oxidation number of a molecule, atom, or ion changes by acquiring or losing an electron is referred to as an oxidation-reduction reaction. Decomposition Reaction is one of the several redox reactions.
This is the redox reaction's overall cell potential. Cd2+ + 2Hg Cd + Hg22+. Both Cd2+ + 2e Cd(s) -0.40 and Hg22+ + 2e 2Hg(l) 0.79
Reduction describes the increase in electrons. Oxidation and reduction always occur jointly because any loss of electrons by one substance must be followed by a gain of electrons by another.
Therefore, oxidation-reduction processes or simply redox reactions are other names for electron-transfer events.
Learn more about redox reactions here brainly.com/question/8727728.
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An increase in the temperature will speed up the reaction by increasing the frequency and efficiency of the collisions of molecules.
Answer:
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