O2H Group
Brenntag Ingredients India Interview Questions and Answers
Q1. Bromintion on aniline and toluene what will be desired product?
The desired product of bromination on aniline is 2,4,6-tribromoaniline. The desired product of bromination on toluene is bromotoluene.
Bromination on aniline results in the substitution of three bromine atoms on the aromatic ring, yielding 2,4,6-tribromoaniline.
Bromination on toluene results in the substitution of one bromine atom on the aromatic ring, yielding bromotoluene.
Q2. 1.How to convert ester to aldehyde?
Esters can be converted to aldehydes by hydrolysis under acidic conditions.
Esters can be hydrolyzed to aldehydes using a strong acid, such as sulfuric acid or hydrochloric acid.
The reaction involves the cleavage of the ester bond and the formation of a carboxylic acid intermediate, which is then further reduced to an aldehyde.
The reaction can be carried out at elevated temperatures or using a catalyst, such as p-toluenesulfonic acid.
For example, ethyl acetate can be converted...read more
Q3. Griganard reaction on aldehyde what will be a product,
The Grignard reaction on an aldehyde will produce a secondary alcohol.
The Grignard reaction involves the addition of a Grignard reagent (organomagnesium compound) to an aldehyde or ketone.
The reaction proceeds through the formation of a carbon-carbon bond.
In the case of an aldehyde, the product will be a secondary alcohol.
For example, the reaction of formaldehyde (HCHO) with a Grignard reagent such as methylmagnesium bromide (CH3MgBr) will yield isopropyl alcohol (CH3CH(OH)CH...read more
Q4. What is the mathod for prepration of amide?
The method for preparation of amide involves the reaction between a carboxylic acid and an amine.
Amides can be prepared by the reaction of a carboxylic acid with an amine in the presence of a dehydrating agent.
The reaction typically requires heating and can be catalyzed by an acid or base.
The resulting product is an amide, which contains a carbonyl group bonded to a nitrogen atom.
Example: The preparation of acetamide can be achieved by reacting acetic acid with ammonia in the...read more
Q5. How will be synthesised biaryl product?
The biaryl product can be synthesized through a variety of methods.
One common method is the Suzuki-Miyaura cross-coupling reaction.
Another method is the Buchwald-Hartwig amination reaction.
Transition metal-catalyzed C-H activation can also be used.
Examples of biaryl products include biphenyl and terphenyl.
Q6. Mass spectra of bromo chloro containing compuond
Mass spectra of bromo chloro containing compound
Bromo chloro compounds can have multiple isomers with different mass spectra
The presence of bromine and chlorine atoms can cause fragmentation in the mass spectrum
The mass spectrum can be used to determine the molecular weight and structural information of the compound
Q7. What is Diasteromer and enansiomer
Diastereomers and enantiomers are types of stereoisomers that differ in their spatial arrangement.
Diastereomers are stereoisomers that have different configurations at one or more chiral centers but are not mirror images of each other.
Enantiomers are stereoisomers that are non-superimposable mirror images of each other.
Diastereomers have different physical and chemical properties, while enantiomers have identical physical properties but may differ in their biological activity...read more
Q8. Proton Nmr peak of methyl aldehyde
The proton NMR peak of methyl aldehyde appears as a singlet at around 9-10 ppm.
The proton NMR spectrum of methyl aldehyde shows a singlet peak.
The chemical shift of the peak is typically around 9-10 ppm.
The singlet peak indicates that the methyl aldehyde molecule has no neighboring protons.
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