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Acetone plus CH3MgBr then H3O

Updated: 5/23/2024
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12y ago

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produces t-butyl alochol. any good organic chemistry text or/and lab book should have similar reactions in a section or grinard reactions.

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12y ago
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4d ago

When acetone reacts with CH3MgBr (methyl magnesium bromide), the carbon atom of the CH3MgBr nucleophilically attacks the carbonyl carbon of the acetone, forming a tertiary alcohol after protonation with H3O+. This reaction is a Grignard reaction, commonly used for carbon-carbon bond formation.

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Q: Acetone plus CH3MgBr then H3O
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Related questions

What substance is the conjugate acid in the reaction HBr plus H2O H3O plus plus Br?

H3o+


Is H3O plus behaving as an acid or base in the following reaction H3PO4 plus H2O H2PO4- plus H3O plus?

In this reaction H3O+ is the conjugate acid. The original acid in this reaction is H3PO4


Is h3o plus acid or base?

H3O is a strong acid.


What are H3O plus units called?

Hydronium ions have the formula H3O+


H3O plus is a polar or nonpolar molecule?

H2O is a polar molecule; +H3O is even more so.


Is H3O plus alkaline?

No, H3O+ (hydronium ion) is acidic. The presence of H3O+ in a solution indicates it is acidic in nature.


Is h3o plus an electriphile?

yes


What is the base of H3O plus is water or not?

The base of H3O+ is water. H3O+ is the hydronium ion, which forms when a water molecule gains a proton. This makes water the base in this reaction.


Is H3O plus a coordinate covalent?

No, H3O+ is not a coordinate covalent bond. It is a hydronium cation formed by the combination of a water molecule and a proton, and it has a regular covalent bond between the oxygen and the hydrogen atoms.


Copper plus water equals?

Cu+ H2O [OH + H3O= 2H2O]Copper plus more than one water = [CuOH + H3O]


What are the concentrations of H3O plus and OH in pure water?

H3O= 0.9 mol/dm3 OH=1.2 mol/dm3


Which of the species below is not basic enough to deprotonate a terminal alkyne CH3Li CH3ONa CH3MgBr CH3Li and CH3MgBr or all of these?

CH3MgBr is not basic enough to deprotonate a terminal alkyne. Its reactivity with terminal alkynes is limited compared to organolithium compounds or sodium alkoxides.