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Class 10 Chemistry: Carbon Compounds Notes

The document discusses carbon and its compounds. It describes how carbon forms covalent bonds by sharing electrons rather than ionic bonds. It discusses the three allotropes of carbon: diamond, graphite, and fullerene. It also describes hydrocarbons and how carbon can form chains, rings, and branches. Functional groups determine the properties of carbon compounds. Nomenclature and chemical properties such as combustion, oxidation, addition and substitution reactions are also summarized.
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0% found this document useful (0 votes)
31 views9 pages

Class 10 Chemistry: Carbon Compounds Notes

The document discusses carbon and its compounds. It describes how carbon forms covalent bonds by sharing electrons rather than ionic bonds. It discusses the three allotropes of carbon: diamond, graphite, and fullerene. It also describes hydrocarbons and how carbon can form chains, rings, and branches. Functional groups determine the properties of carbon compounds. Nomenclature and chemical properties such as combustion, oxidation, addition and substitution reactions are also summarized.
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© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Delhi Public School-Bopal, Ahmedabad

Class 10
Chapter 4 Carbon and its compounds Notes

Covalent Bond: The atomic number of carbon is 6. Its electronic configuration is 2, 4. It


requires, 4 electrons to achieve the inert gas electronic configuration. But carbon cannot form
an ionic bond

It could gain four electrons forming C4- cation. But it would be difficult for the nucleus with
six protons to hold on to ten electrons.

It could lose four electrons forming C4+ cations. But it requires a large amount of energy to
remove four electrons.

Thus, carbon overcomes this problem by sharing of its valence electrons with other carbon
atoms or with atoms of other elements.

The bond formed by mutual sharing of electron pairs between two atoms in a molecule is
known as Covalent Bond.

• Single Covalent Bond: When a single pair of electrons are shared between two atoms
in a molecule. For example; F2, Cl2, H2 etc.
• Double Covalent Bond: When two pairs of electrons are shared between two atoms in
a molecule. For example; O2, CO2 etc.
• Triple Covalent Bond: When three pairs of electrons are shared between two atoms in
a molecule. For example; N2 etc.

Allotropes of Carbon
Different forms of an element that have the same chemical properties but different
physical properties are known as Allotropes. There are three allotropes of carbon-
diamond, graphite and fullerene.

Diamond
Diamond exists as a three-dimensional network with strong carbon-carbon covalent
bonds. Diamonds are hard in nature with high melting points. It shines in the presence
of light and it is a bad conductor of electricity. The most common use of diamonds is
in making jewellery. It is also used in cutting and drilling tools.

Graphite
Graphite is made from weak Van der Waal forces. Each carbon atom is bonded wit h
the other three carbon atoms to form hexagonal rings. It serves as a good conductor of
heat and electricity. It is used as a dry lubricant for machine parts as well as it is used
in lead pencils.

Fullerene
It is a hollow cage that exists in the form of a sphere. Its structure is similar to
fullerene. But along with hexagonal rings, sometimes pentagonal or heptagonal rings
are also present.

Fig.1 Structure of fullerene

Two Important Properties of Carbon


Catenation and tetravalency are the two important properties of carbon. Catenation is
a property of carbon by which carbon atoms can link one another via the covalent
bonds and can form long chains, closed rings or branched chains etc. Carbon atoms
can be linked by single, double or triple bonds. Carbon has a valency of 4 due to
which it is known to have tetravalency. Due to this one carbon atom can bond with
other 4 carbon atoms, with other atoms also such as Oxygen, Nitrogen etc.

Hydrocarbons
Compounds that are made up of carbon and hydrogen are known as Hydrocarbons.
There are two types of hydrocarbons found - Saturated
Hydrocarbons and Unsaturated Hydrocarbons. Saturated Hydrocarbons consist of
single bonds between the carbon atoms. For Example, Alkanes. Alkanes are saturated
hydrocarbons represented by a formula, CnH2n+2.
Unsaturated Hydrocarbons are the ones with double or triple bonds between the
carbon atoms. For Example, Alkenes and Alkynes. Alkenes are represented as
CnH2n whereas alkynes are represented as CnH2n-2. Some saturated hydrocarbons
and unsaturated hydrocarbons are represented as -
Fig.2. Saturated hydrocarbons

Fig. 3. Unsaturated hydrocarbons


The structure of hydrocarbons can be represented in the form of electron dot structure
as well as open structures as shown below-

Fig.4. Electron dot structure and open structure of ethane


Fig.5. Electron dot structure and open structure of ethyne

Carbons Compounds based on the structure


Carbon Compounds can be classified as straight-chain compounds, branched-chain
compounds and cyclic compounds. They are represented as -

Fig.6. Straight chain carbon compound

Fig.7. Branched-chain compounds


Fig.8. Cyclic carbon compounds

Functional Groups
One of the hydrogen atoms in hydrocarbons can be replaced by other atoms according
to their valencies. The atoms which decide the properties of the carbon atoms are
known as Functional Groups. For Example, Cl, Br, -OH, Aldehyde, Ketone,
Carboxylic Acid etc.

Homologous Series
Series of compounds in which the same functional group substitutes f or the hydrogen
atom in a chain of carbon.

Fig.9. Homologous series

Nomenclature of Carbon Compounds


• First of all, identify the number of carbon atoms in compounds. And in it
identify the longest chain
• Then the functional group can be indicated by suffix or prefix.
• Cyclic hydrocarbon is designated by the prefix cyclo.
• If there are two or more different substituents they are listed in alphabetical
order
Fig.10. Different functional groups

Chemical Properties of Carbon Compounds

Combustion
Carbon along with its compound is used as a fuel as it burns in presence of oxygen to
release energy. Saturated hydrocarbons produce blue and non -sooty flame whereas
unsaturated hydrocarbons produce a yellow sooty flame.
CH4 + 2O2 → CO2 + 2H2O

Oxidation
Alcohol can be oxidised to aldehydes whereas aldehydes, in turn, can be oxidised to
carboxylic acid. Oxidising agents such as potassium permanganate can be used for
oxidation.
Addition Reaction
Hydrogenation of vegetable oil is an example of an additional reaction. Addition of
hydrogen in presence of catalysts such as nickel or palladium. This converts the oil
into ghee.

Substitution Reaction
When one atom in hydrocarbon is replaced by chlorine, bromine, etc. this is known as
a Substitution Reaction.

Important Carbon Compounds: Ethanol and Ethanoic Acid


Ethanol is a volatile liquid with a low melting point. It reacts with sodium to form
sodium ethoxide.

This reaction is used to test the presence of ethanol by the evolution of hydrogen gas.
Dehydration of ethanol in presence of hot sulphuric acid forms alkene.

Ethanoic acid is a colourless liquid. When pure ethanoic acid freezes like ice, it is
known as Glacial Acetic Acid. It is formed at a temperature of about 16.6 degrees
centigrade
Ethanoic Acid/Acetic acid when reacts with ethanol forms an ester. Ester can be
identified by its sweet smell.

The reaction of esters with a strong base is used to form soap. This is known
as Saponification. Acetic acid also reacts with a strong base to form sodium acetate
and water.
NaOH + CH3COOH + CH3COONa + H2O

Soaps and Detergents


Sodium or potassium salt of a carboxylic acid is known as Soap. They work most
effectively in soap water. Detergents are sulphonate or ammonium salt of a long chain
of carboxylic acid. They can work effectively on soft as well as hard water.

Cleansing Action of Soaps and Detergents


The cleansing action of soaps and detergents is due to the ability to minimise the
surface tension of water, to emulsify oil or grease and hold them in a suspension of
water. When soap dissolves in water, it forms soap anions and soap cations. The
hydrophobic part of soaps and detergents are soluble in grease and the hydrophilic
part is soluble in water.

Soap and Micelle Formation


When dirt and grease are mixed with soap water, soap molecules arrange them in tiny
clusters known as Micelle. The hydrophilic part sticks to the water and forms the
outer surface of the micelle and the hydrophobic part binds to oil and g rease.

Common questions

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Saturated hydrocarbons contain single bonds between carbon atoms, as seen in alkanes (e.g., ethane) represented by CnH2n+2. Unsaturated hydrocarbons have double or triple bonds, with alkenes represented as CnH2n (e.g., ethene) and alkynes as CnH2n−2 (e.g., ethyne).

Functional groups determine the properties and reactivity of carbon compounds by replacing hydrogen atoms, thus defining the chemical behavior and classification. For instance, OH groups transform hydrocarbons into alcohols, while carbonyl groups form aldehydes and ketones, significantly altering solubility and reactivity .

The reaction of ethanol with sodium, forming sodium ethoxide and hydrogen gas, indicates its reactivity as a reducing agent. Its dehydration forms ethene, showing potential as a precursor in industrial synthesis for producing ethylene-based compounds, emphasizing its versatility as an industrial feedstock .

Soaps, being sodium or potassium salts of carboxylic acids, work best in soft water but are less effective in hard water due to mineral ion interference. Detergents, which are sulphonate or ammonium salts, remain effective in both soft and hard water due to their synthetic surfactant properties that prevent calcium and magnesium ions in hard water from precipitating .

Catenation allows carbon atoms to form long chains, branched or closed rings through covalent bonds. This, along with tetravalency, enables carbon to form a vast number of compounds by bonding with four other atoms, including other carbon atoms, contributing to the diversity and complexity of organic chemistry .

Saponification involves the reaction of esters, such as triglycerides in fats, with strong bases like NaOH. This reaction results in the formation of soap and glycerol. The base hydrolyzes the ester bonds, yielding the sodium salt of fatty acids (soap) and removing glycerol, which acts as a by-product .

Diamond has a three-dimensional network with strong carbon-carbon covalent bonds, making it hard and a poor conductor of electricity. Graphite consists of layers held by weak Van der Waals forces, allowing it to conduct electricity and making it a good lubricant. Fullerene forms spherical hollow cages with combinations of hexagonal, pentagonal, or heptagonal rings which contributes to unique properties among the allotropes .

Carbon has an electronic configuration of 2, 4, needing four electrons to achieve a stable, inert gas configuration . However, forming ionic bonds is not feasible because gaining or losing four electrons to form C4- or C4+ ions is energetically unfavorable. The nucleus would struggle to maintain ten electrons as a C4- ion and losing four electrons requires significant energy, making covalent bonding more practical where the atoms share electrons .

Saturated hydrocarbons, like methane, produce a blue and non-sooty flame, while unsaturated hydrocarbons yield a yellow sooty flame due to incomplete combustion. The combustion of methane can be represented by the reaction: CH4 + 2O2 → CO2 + 2H2O .

Micelle formation occurs when soap molecules arrange themselves in spherical clusters. The hydrophobic tails dissolve in grease/oil, while the hydrophilic heads face outward towards water. This dual nature helps emulsify the grease and hold it in suspension, allowing it to be rinsed away with water .

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