Phenylmagnesium bromide is often used as a substitute for the phenylene “Ph” synthon. To start the reaction, laboratory preparations include treating bromobenzene with magnesium metal, usually in the form of turnings. The brombenzene reaction makes the compound ready to give benzone. It is a Grignard reagent used in the synthesis of phenyl-phenol synchronized chemistry.
Which Of The Following Compound Formed When Phenyl Magnesium Bromide Reacts With Tertiary Butanol?
Phenyl Magnesium Bromide responds with tert. Butanol, benzene, is also available as a drug.
The molecule, Phenyl magnesium bromide, is more commonly represented as C6H5MgBr, and it is a magnesium-containing organometallic compound.
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The reaction is as follows: Alcoholic beverages from the OH group are linked to active hydrogenation.
B.B.is B, the correct option. – B. Aryl (or alkyl) is the correct option for the benzene product, according to the Grignard reagent.
What Will Be The Product Formed When Acetone Is Treated With Phenyl Magnesium Bromide?
The acetone produced by reacting with another molecule of phenyl magnesium bromide to produce dimethyIphenol carblno.