Answer:
Pentan-2-ol
Explanation:
On this reaction, we have a <u>Grignard reagent</u> (ethylmagnesium bromide), therefore we will have the production of a <u>carbanion</u> (step 1). Then this carbanion can <u>attack the least substituted carbon</u> in the epoxide in this case carbon 1 (step 2). In this step, the epoxide is open and a negative charge is generated in the oxygen. The next step, is the <u>treatment with aqueous acid</u>, when we add acid the <u>hydronium ion</u> (
) would be produced, so in the reaction mechanism, we can put the hydronium ion. This ion would be <u>attacked by the negative charge</u> produced in the second step to produce the final molecule: <u>"Pentan-2-ol".</u>
See figure 1
I hope it helps!
Answer:
In the attached photo.
Explanation:
Hello,
You could find the structure in the attached photo, taking into account that the initial (Z) resembles to the trans arrangement for this alkene.
Best regards.
Volume ⇒ 50 mL in liters : 50 / 1000 = 0.05 L
Molarity of solution ⇒ 0.15 M
Number of moles:
n = M * V
n = 0.15 * 0.05
n = 0.0075 moles of CuCl2
hope this helps!.
Limiting Reactant - The reactant in a Chemical Reaction that limits the amount of product that can be formed.
Excess Reactant - The reactant in a chemical reaction that remains when a reaction stops when the limiting reactant is completely consumed.
Theoretical Yield - The quantity of a product obtained from the complete conversion of the limiting reactant in a Chemical reaction.
I hope this helped make your question easier ^_^
