CHPATER- 4 CARBON AND ITS COMPOUNDS
NOTES
- The shared pair of electrons between two hydrogen atoms forms a single covalent bond.
- In covalent bond molecules, the intramolecular bonds are strong, but the intermolecular forces are weak.
- These compounds have low boiling and melting points due to weak intermolecular forces.
- Due to the nature of covalent bonding, carbon has the ability to form a large number of compounds.
- Saturated Compounds– Carbon compounds in which carbon atoms are connected only by single bonds are called saturated compounds.
- Unsaturated Compounds– Carbon compounds that contain double or triple bonds between carbon atoms are called unsaturated compounds.
- The extent of catenation found in carbon compounds is not observed in any other element.
- To obtain the structure of simple carbon compounds, carbon atoms are first linked together by single bonds. Then, hydrogen atoms are added to satisfy the remaining valency of carbon. Example: Ethane (C₂H₆)
Each carbon atom has three unsatisfied valencies, so each carbon forms bonds with three hydrogen atoms to fulfill its valency.
- All atoms satisfy their valency through single bonds in these compounds. Such compounds are called saturated compounds. They are less reactive.
Carbon compounds that have double or triple bonds between carbon atoms are called unsaturated carbon compounds, and they are more reactive compared to saturated carbon compounds.
Compounds that have the same molecular formula but different structures are called structural isomers.
Heteroatoms and the functional groups in which they are present impart specific properties to compounds. These properties do not depend on the length or nature of the carbon chain; hence, they are called functional groups.
When the molecular mass increases in a homologous series, a gradual variation in physical properties is observed.
The solubility, as a physical property, also shows a similar trend in a particular solvent. However, the chemical properties, which are fully determined by the functional group, remain consistent within a homologous series.
A) To determine the number of carbon atoms in a compound, identify the carbon chain. A compound with three carbon atoms will be named propane.
B) The presence of the functional group is indicated in the compound's name with a prefix or suffix, depending on its position and nature.
C) If the name of the functional group is to be given based on a suffix and the name of the functional group begins with a vowel (a, e, i, o, u), then the last 'e' from the carbon chain name is dropped, and the appropriate suffix is added to modify the name.
D) In an unsaturated carbon chain, the final "ane" in the name of the carbon chain is replaced with "ene" or "yne," depending on whether there is a double or triple bond, respectively.
17. Chemical properties of carbon compounds-
a) Combustion– In all its allotropes, carbon burns in oxygen to produce carbon dioxide along with heat and light. During combustion, most carbon compounds also release a significant amount of heat and light.
C + O₂ → CO₂ + heat and light
b) Oxidation– Some substances have the ability to give oxygen to other substances. These substances are called oxidizing agents.
- Alkaline potassium permanganate or acidified potassium dichromate oxidize alcohols into acids, meaning they add oxygen to the starting substance.
c) Addition Reaction– In the presence of catalysts like palladium or nickel, unsaturated hydrocarbons add hydrogen to form saturated hydrocarbons. Catalysts are substances that cause a reaction to proceed at a different rate without being consumed or altered in the reaction. The hydrogenation of vegetable oils is typically carried out using nickel as a catalyst in this type of reaction.
d) Substitution Reaction– In the presence of sunlight, a very fast reaction occurs in which chlorine gets added to the hydrocarbon. Chlorine replaces the hydrogen atoms one by one. This type of reaction is called a substitution reaction.
18. Ethanol and acetic acid-
Properties of Ethanol– Ethanol is in a liquid state at room temperature. It is called alcohol and is an important component of all alcoholic beverages. It is also a good solvent.
- It is used in medicines such as tincture of iodine, cough syrup, tonic, etc.
Reactions of ethanol-
a) Reaction with sodium-
2Na+2CH3CH2OH→2CH3CH2O−Na++H2
Alcohol reacts with sodium to release hydrogen gas. In the reaction with ethanol, the second product formed is sodium ethoxide.
b) Reaction to form unsaturated hydrocarbons– When ethanol is heated with concentrated sulfuric acid at 443K, dehydration of ethanol occurs, resulting in the formation of ethene.
CH3CH2OH→CH2=CH2+H2O
In this reaction, sulfuric acid acts as a dehydrating agent, which removes water from ethanol.
Properties of Acetic Acid– Acetic acid is commonly known as vinegar and is related to the carboxylic acid group.
- A 3-4% solution of acetic acid is called vinegar, and it is used as a preservative in pickles.
- The melting point of pure acetic acid is 290K, and therefore, in cold climates during the winter, it freezes. For this reason, it is called glacial acetic acid.
Reactions of acetic acid-
a) Esterification Reaction– Esters are primarily formed by the reaction of an acid and an alcohol. Acetic acid reacts with pure ethanol in the presence of an acid catalyst to form an ester.
CH3COOH+CH3CH2OH⇌CH3COOCH2CH3+H2O
- By reacting with sodium hydroxide, which is a base, an ester is converted back into an alcohol and the sodium salt of the carboxylic acid. This reaction is called saponification.
- CH3COOC2H5+NaOH→C2H5OH+CH3COONa
Soap molecules are sodium and potassium salts of long-chain fatty acids. The ionic part of soap interacts with water, while the carbon chain interacts with oil.
Soap molecules have two ends with different properties. The end that is soluble in water is called the hydrophilic end, and the other end, which is soluble in hydrocarbons, is called the hydrophobic end.