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Converting \(\mathrm{n}\) -hexane into benzene in the presence of chromium oxide on alumina support is an example of (1) hydrogenation reaction (2) isomerisation reaction (3) aromatisation reaction (4) substitution reaction

Short Answer

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(3) aromatisation reaction

Step by step solution

01

Identify the Reaction Type

Converting n-hexane (a straight-chain alkane) into benzene (an aromatic compound) involves changing the structure and properties of the molecule.
02

Define Reaction Options

Hydrogenation reaction adds hydrogen to a compound. Isomerisation changes the structure of a molecule without changing its molecular formula. Aromatisation converts alkanes to aromatic compounds. Substitution replaces one atom or group in a molecule with another.
03

Determine the Correct Option

Since the process involves converting an alkane (n-hexane) to an aromatic compound (benzene), the correct type of reaction must involve creating an aromatic structure.
04

Select the Correct Answer

The correct type of reaction is the one that converts alkanes to aromatic compounds, which is an aromatisation reaction.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

organic chemistry
Organic chemistry is the branch of chemistry that deals with the study of carbon-containing compounds.
It covers a wide range of substances, including hydrocarbons, alcohols, acids, and more complex molecules found in living organisms.

Studying organic chemistry helps us understand the structure, properties, and reactions of these molecules, which is crucial for fields like medicine, agriculture, and materials science.
A key aspect is learning about different types of organic reactions.
For example, in our given exercise, we look at the aromatisation reaction, where a simple alkane is transformed into a more complex aromatic compound.
reaction mechanisms
Understanding reaction mechanisms is essential to mastering organic chemistry.
A reaction mechanism explains the step-by-step process through which reactants turn into products.
It involves details like intermediate steps, transition states, and the energy changes that occur.

In the context of our exercise, the conversion of n-hexane to benzene involves several intermediate steps:
  • First, the n-hexane may undergo dehydrogenation, removing hydrogen atoms.
  • Then, it undergoes cyclization, forming a ring structure.
  • Finally, it may undergo further dehydrogenation to form the aromatic benzene.
These steps are facilitated by a catalyst, such as chromium oxide on alumina, which helps in speeding up the reaction without being consumed.
hydrocarbons conversion
Hydrocarbons conversion refers to the process of transforming one type of hydrocarbon into another.
This includes reactions like cracking, reforming, and in our exercise, aromatisation.

Aromatisation is a specific type of hydrocarbon conversion where alkanes are converted into aromatic compounds.
This process is particularly important in the petrochemical industry for producing valuable chemicals.

Let's break down the aromatisation of n-hexane to benzene:
  • Chromium oxide on alumina acts as a catalyst.
  • n-Hexane, a straight-chain alkane with 6 carbon atoms, loses hydrogen atoms in a dehydrogenation step.
  • It then undergoes cyclization, forming a six-membered carbon ring.
  • Finally, it loses additional hydrogen atoms to form benzene, a stable aromatic compound.
The entire process significantly enhances the value of the original hydrocarbon by converting it into a more useful and versatile chemical.

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Most popular questions from this chapter

Which of the following alkanes cannot be synthesised by the Wurtz reaction in good yield? (1) \(\left(\mathrm{CII}_{3}\right)_{2} \mathrm{CII} \mathrm{CII}_{2} \mathrm{CII}\left(\mathrm{CII}_{3}\right)_{2}\) (2) \(\left(\mathrm{CII}_{3}\right)_{2} \mathrm{CII} \mathrm{CII}_{2} \mathrm{CII}_{2} \mathrm{CII}\left(\mathrm{CII}_{3}\right)_{2}\) (3) \(\mathrm{CII}_{3} \mathrm{CII}_{2} \mathrm{C}\left(\mathrm{CII}_{3}\right)_{2} \mathrm{CII}_{2} \mathrm{CII}_{3}\) (4) \(\left(\mathrm{CII}_{3}\right)_{3} \mathrm{C} \mathrm{CII}_{2} \mathrm{CII}_{2} \mathrm{CII}_{3}\)

Which of the following alkenes on catalytic hydrogenation yield 2 -methyl pentane? (1) 4 -methyl-1-pentene (2) 4 -methyl pentene-2 (3) 2 -methyl pentene-2 (4) 2 -methyl pentene-1 (5) All of the above

The treatment of \(\mathrm{CH}_{3} \mathrm{Mg} \mathrm{X}\) with \(\mathrm{CH}_{3}-\mathrm{C} \equiv \mathrm{CH}\) produces (1) \(\mathbf{C H}_{4}\) (2) \(\mathrm{CH}_{3} \mathrm{CH}=\mathrm{CH}_{2}\) (3) \(\mathrm{CH}_{3} \mathrm{C} \equiv \mathrm{CCH}_{3}\) (4) \(\mathbf{C H}_{3} \mathrm{CH}=\mathrm{CHCH}_{3}\)

Which of the following will not produce ethane? (1) reduction of \(\mathrm{CH}_{3} \mathrm{COOH}\) with \(\mathrm{HI}\) and red \(\mathrm{P}\) (2) reduction of \(\mathrm{CH}_{3} \mathrm{COCH}_{3}\) with HI and red \(\mathrm{P}\) (3) soda lime decarboxylation of sodium propionate (4) hydrogenation of ethene in the presence of Raney nickel

Which of the following statements is wrong? (1) In the halogenation of alkanes, \(3^{\circ}\) II is more reactive (2) Nbstraction of \(3^{\circ}\) II in alkanc leads to the generation of most stable \(3^{\circ}\) radical (3) \(3^{\circ}\) alkyl radical is gencrated slowcr than \(1^{\circ}\) and \(2^{\circ}\) radicals (4) Bromination of alkanes is most selective

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