subject
Chemistry, 03.12.2021 01:50 ajbrock1004

One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give new carbon-carbon bonds. In this reaction, the carbon of the organometallic compound acts as a nucleophile to add to the positive carbon of the carbonyl forming an alkoxide ion intermediate. Aqueous acid is used in the second step to protonate the alkoxide ion and form the product alcohol. Draw the structure of the product(s) of step 2 when the following compound reacts with phenylmagnesium bromide.

ansver
Answers: 3

Another question on Chemistry

question
Chemistry, 21.06.2019 23:00
What is the formula that this ionic compounds could form sr2+p3-o2-
Answers: 3
question
Chemistry, 22.06.2019 07:10
Provide a stepwise curved arrow mechanism that fully explains the outcome of the reaction shown below. oh нао* heat он
Answers: 2
question
Chemistry, 23.06.2019 08:10
Time remaining 58: 10 an atom that has 84 protons and 86 neutrons undergoes a reaction. at the end of the reaction, it has 82 protons and 84 neutrons. what happened to the atom? it accepted radiation in a chemical reaction it donated neutrons to another atom in a chemical reaction it emitted an alpha particle in a nuclear reaction. it accepted protons in a nuclear reaction. mark this and retum save and exit next submit
Answers: 3
question
Chemistry, 23.06.2019 09:00
What properties would have caused early researchers to name hydrogen "inflammable air”
Answers: 3
You know the right answer?
One of the most important uses for Grignard reagents is their addition to carbonyl compounds to give...
Questions
question
Mathematics, 26.03.2021 05:50
question
Mathematics, 26.03.2021 05:50
question
Mathematics, 26.03.2021 05:50
question
Mathematics, 26.03.2021 05:50
question
Mathematics, 26.03.2021 05:50
question
Mathematics, 26.03.2021 05:50