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Maximum ability of catenation is shown by: (a) Sulphur (b) Nitrogen (c) Oxygen (d) Carbon

Short Answer

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Carbon (d) shows the maximum ability of catenation.

Step by step solution

01

Understand the concept of catenation

Catenation is the ability of an element to form chains with atoms of the same element. It is primarily observed in carbon due to its tetravalency and the strong bond it can form with other carbon atoms. Besides carbon, elements like sulfur, nitrogen, and oxygen can also exhibit catenation but to a lesser extent.
02

Evaluate catenation in each element

- **Sulphur**: Can form long chains known as polysulfides, but these chains are much less stable than carbon chains. - **Nitrogen**: Can form N-N bonds but is not stable in long chains due to weak N-N bonds. - **Oxygen**: Mostly forms O-O linkages in peroxides but is typically less stable in long chains. - **Carbon**: Due to its ability to form strong C-C bonds and diversify into various structures like chains, rings, and networks, it shows maximum catenation.
03

Compare and conclude

Carbon's ability to form various long chains, branched chains, and three-dimensional structures (such as graphite and diamond) make it the element with maximum catenation. The versatility and strength of C-C bonding surpass the catenation abilities of sulfur, nitrogen, and oxygen.

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Key Concepts

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

Carbon bonding
Carbon bonding is a fundamental concept in chemistry that showcases how carbon atoms connect with others to form diverse structures. The uniqueness of carbon comes from its ability to create strong covalent bonds with many elements, especially with other carbon atoms. This capability plays a vital role in forming complex molecules.

Carbon atoms bond by sharing electrons, which leads to the formation of single, double, or triple bonds. Each type of bond has different energy levels and lengths, contributing to the structures' stability and strength. For example, single bonds are flexible and allow for rotation, making the carbon chains versatile.

  • Single Bonds: Provide flexibility, allowing chains to rotate.
  • Double Bonds: Create rigidity, as they prevent rotation around the bond.
  • Triple Bonds: Result in even stronger and shorter bonds.
Carbon can form various structures such as chains, rings, or networks, which is why it is considered the backbone of organic chemistry. With such diverse bonding capabilities, carbon forms the foundation of life's molecular complexity.
Tetravalency of carbon
The tetravalency of carbon is a crucial aspect that allows for its extensive bonding capabilities. Tetravalency means that a carbon atom has four electrons available to form bonds, resulting in a valence of four.

This property enables carbon to share its four electrons with other atoms to create stable and robust covalent bonds. By equitably distributing these electrons, carbon can connect with several other carbon atoms or different elements like hydrogen, oxygen, nitrogen, and sulfur, forming a vast array of compounds.

  • Valence electrons: Four, allowing for numerous possible connections.
  • Covalent bonds: Formed by sharing electrons, resulting in strong chemical linkages.
  • Variety: Tetravalency accounts for carbon’s ability to take on multiple functional groups and structural forms.
This versatility in bonding is what drives carbon's central role in organic molecules, providing the structural diversity necessary for complex life forms and synthetic compounds alike.
Stability of chains
The stability of carbon chains is an important factor that distinguishes carbon from other elements capable of catenation. Carbon chains are stable due to the strong covalent bonds formed between carbon atoms. This strength arises due to both the optimal overlap of atomic orbitals and the high bond dissociation energy involved in carbon-carbon bonds.

The unique strength and stability of carbon-based chains allow for the formation of extensive carbon structures. Some key aspects contributing to chain stability include:

  • Bond Energy: C-C bonds have a higher bond energy than those formed by elements like nitrogen or oxygen.
  • Overlap: The sp³ hybridization in single carbon bonds contributes to chain robustness.
  • Versatility: Allows for complex branching and cross-linking.
These properties not only enable carbon to form long-lasting chains but also permit these chains to assume various configurations like straight, branched, or cyclic forms. This adaptability and resilience of carbon chains underpin the vast number of organic compounds, influencing fields ranging from biochemistry to industrial chemistry.

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Most popular questions from this chapter

Boron compounds behave as lewis acids because of their (a) Ionisation energy (b) Electron deficient nature (c) Covalent nature (d) Ionisation energy

In diborane (a) 2 -bridged hydrogens and four terminal hydrogens are present. (b) 3 -bridged hydrogens and three terminal hydrogens are present. (c) 4 -bridged hydrogens and two terminal hydrogens are present. (d) None of the above.

Which of the following statement is/are correct? (1) \(\mathrm{B}(\mathrm{OH})_{3}\) reacts with \(\mathrm{NaOH}\), forming \(\mathrm{Na}\left[\mathrm{B}(\mathrm{OH})_{4}\right]\). (2) \(\mathrm{B}(\mathrm{OH})_{3}\) does not donate a proton and hence does not form any salt with \(\mathrm{NaOH}\) (3) \(\mathrm{B}(\mathrm{OH})_{3}\) partially reacts with water to form \(\mathrm{H}_{3} \mathrm{O}^{+}\) and \(\left[\mathrm{B}\left(\mathrm{OH}_{4}\right)^{-}\right]\) and behaves like a weak acid (4) \(\mathrm{B}(\mathrm{OH})_{3}\) behaves like a strong monobasic acid in presence of sugars and this acid can be titrated against an \(\mathrm{NaOH}\) solution using phenolphthalein as an indicator. (a) \(1,2,3\) (b) \(2,3,4\) (c) 2,3 (d) \(1,3,4\)

Aluminium is more reactive than iron because its standard reduction potential is higher. Still aluminium is less easily corroded than iron because (a) Al reacts with atmospheric carbon dioxide to form a self protective layer of \(\mathrm{Al}_{2} \mathrm{O}_{3}\). (b) it has higher reducing power and forms a self protective layer of \(\mathrm{Al}_{2} \mathrm{O}_{3}\). (c) it has higher reducing power and does not react with oxygen so easily. (d) Both (A) and (B)

Boric acid is polymeric due to (a) Its geometry (b) Its presence of hydrogen bonds (c) Its acidic nature (d) Its monobasic nature

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