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Brenntag Ingredients India Interview Questions and Answers

Updated 5 Feb 2024

Q1. Bromintion on aniline and toluene what will be desired product?

Ans.

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.

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Q2. 1.How to convert ester to aldehyde?

Ans.

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

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Q3. Griganard reaction on aldehyde what will be a product,

Ans.

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

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Q4. What is the mathod for prepration of amide?

Ans.

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

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Q5. How will be synthesised biaryl product?

Ans.

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.

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Q6. Mass spectra of bromo chloro containing compuond

Ans.

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

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Q7. What is Diasteromer and enansiomer

Ans.

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

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Q8. Proton Nmr peak of methyl aldehyde

Ans.

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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