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What by products would you expect from the nitration of methyl benzoate?
Benzoate indicates a COO- group attached to the benzene ring. This is a deactivating group and deactivates the benzene ring as well as is a meta directing group. Hence, two products could form. 1. Monosubstitution - results in 3-nitromethylbenzoate 2. Disubstitution - results in 3,5-dinitromethylbenzoate
What product is generated by the reaction of methyl benzoate with dilute sulphuric acid?
The reaction of methyl benzoate with dilute sulfuric acid generates benzoic acid and methanol as the main products.
What is methyl m-nitrobenzoate molecular weight?
181gMethyl Benzoate is 136gMethyl benzoate is when you replace one of the hydrogens with a group of NO2NO2 has a mass of= 46gadd this to the mass of the methyl benzoate then take away 1 which is mass of the hydrogen that was replaced
What is the procedure for synthesis of 3-nitrobenzaldehyde?
Check the book Macroscale and Microscale by Williamson and Masters. Go to the chapter entitled Nitration of Methyl Benzoate. The synthesis of 3-nitrobenzaldehyde/3-nitrobenzoic acid has the same procedure.
What is the best solvent for methyl benzoate?
The best solvent for methyl benzoate is typically a non-polar solvent such as diethyl ether or dichloromethane. These solvents are effective in dissolving methyl benzoate due to its non-polar nature and facilitate its extraction and purification processes.
What by products would you expect from the nitration of methyl benzoate?
Benzoate indicates a COO- group attached to the benzene ring. This is a deactivating group and deactivates the benzene ring as well as is a meta directing group. Hence, two products could form. 1. Monosubstitution - results in 3-nitromethylbenzoate 2. Disubstitution - results in 3,5-dinitromethylbenzoate
What product is generated by the reaction of methyl benzoate with dilute sulphuric acid?
The reaction of methyl benzoate with dilute sulfuric acid generates benzoic acid and methanol as the main products.
What is the mechanism for the nitration of 4 methylphenol nitric acid with sulfuric acid catalyst?
4 methyl (3, 5 dinitro) phenylol
What is methyl m-nitrobenzoate molecular weight?
181gMethyl Benzoate is 136gMethyl benzoate is when you replace one of the hydrogens with a group of NO2NO2 has a mass of= 46gadd this to the mass of the methyl benzoate then take away 1 which is mass of the hydrogen that was replaced
Is methyl benzoate an ester?
Methyl benzoate, an organic compound, is an ester. It is a colorless liquid that is not soluble in water and has a fruity smells. Some uses for methyl benzoate are as a solvent and a pesticide.
What is the procedure for synthesis of 3-nitrobenzaldehyde?
Check the book Macroscale and Microscale by Williamson and Masters. Go to the chapter entitled Nitration of Methyl Benzoate. The synthesis of 3-nitrobenzaldehyde/3-nitrobenzoic acid has the same procedure.
What is the best solvent for methyl benzoate?
The best solvent for methyl benzoate is typically a non-polar solvent such as diethyl ether or dichloromethane. These solvents are effective in dissolving methyl benzoate due to its non-polar nature and facilitate its extraction and purification processes.
What colour does sulfuric acid turn when you put methyl orange in?
Sulfuric acid will turn red when methyl orange is added, indicating that the solution is highly acidic.
Why hcl don't used in preparation of methyl m nitrobenzoate?
HCl is not used in the preparation of methyl m-nitrobenzoate because the presence of a strong acid like HCl can lead to unwanted side reactions, such as hydrolysis or nitration of other functional groups on the molecule. Instead, a milder acid catalyst like sulfuric acid is typically used in these types of reactions to promote the esterification process efficiently.
What preservative is used to treat edible rose water concentrate to make them last for years?
methyl parabenpropyl parabensodium benzoate
What is the ester formed from octyl benzoate?
The ester formed from octyl benzoate is called octyl benzoate. It is formed when octanol reacts with benzoic acid in the presence of a catalyst. This ester is commonly used in cosmetics and personal care products as a fragrance ingredient or UV filter.
Why to keep temperature low in nitration reaction?
To prevent di-nitration of the methy benzoate because COOMe group attached to the aromatic ring is deacitvating, hence, plus the deactivating NO2 group, a higher temperature and more acidic condition would be required to add another NO2 to the 5th carbon of the aromatic ring of the methyl 3-nitrobenzoate
