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!
An answer befitting your question…
Hi mom, I’m having troubles with my teachers. They are cruel to me and I cannot concentrate. I think if we changed schools it would be much better. Thank you mom.
Answer:
The arrow points from the reactants to the products, so just follow the arrows.
Explanation:
some have the reactants on the left and the products on the right, and others are the opposite... just know that
reactants---------> products
or
products<-----------reactants
Explanation:
SADMEP
-2(bx-5) = 16 distribute
-2bx +10 = 16 subtracte
-10 -10
-2bx = 6
divide by -2x (on both sides)
b = -3x
