produces t-butyl alochol. any good organic chemistry text or/and lab book should have similar reactions in a section or grinard reactions.
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.
H3o+
In this reaction H3O+ is the conjugate acid. The original acid in this reaction is H3PO4
No, H3O+ (hydronium ion) is acidic. The presence of H3O+ in a solution indicates it is acidic in nature.
yes
H3O= 0.9 mol/dm3 OH=1.2 mol/dm3
H3o+
In this reaction H3O+ is the conjugate acid. The original acid in this reaction is H3PO4
H3O is a strong acid.
Hydronium ions have the formula H3O+
H2O is a polar molecule; +H3O is even more so.
No, H3O+ (hydronium ion) is acidic. The presence of H3O+ in a solution indicates it is acidic in nature.
yes
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.
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.
Cu+ H2O [OH + H3O= 2H2O]Copper plus more than one water = [CuOH + H3O]
H3O= 0.9 mol/dm3 OH=1.2 mol/dm3
CH3MgBr is not basic enough to deprotonate a terminal alkyne. Its reactivity with terminal alkynes is limited compared to organolithium compounds or sodium alkoxides.