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.
The answer is E. You must use the formula q=mCDeltaT to solve this equation. You must also use the formula that q(reaction)=q(solution) to solve this problem
A redox reaction be used as a source of electrical energy only when two half-reactions are physically separated. <span>The electrons that are released at the anode flow through the wire, producing an electric current. Galvanic cells therefore transform chemical energy into electrical energy that can then be used to do work.</span>
There are no numbers provided so I will try to explain the equation. If you want to find the percent error you would do theoretical (the number it’s supposed to be) minus experimental (the number you got in the experiment) over the theoretical value (same as the first one.) You must multiply this by 100 in order to show the actual percentage rather than very low decimals. You want the percent error to be as low as possible because the lower it is the less mistakes happened. Mistakes can include too much/less of solvent, solution, or the glassware wasn’t clean enough, and much much more.
I hope this helps!
Please mark the brainliest if it does! (:
Answer:
The deprotonated organic acid (RCO2-) and protonated organic base (RNH3+) go into the aqueous layer because Organic compounds that are neither acids or bases do not react with either NaOH or HCl and, therefore remain more soluble in the organic solvent and are not extracted.
Explanation:
