Courses
Courses for Kids
Free study material
Offline Centres
More
Store Icon
Store

Organic Chemistry Concepts Reactions and Mechanisms

ffImage
banner

What Is Organic Chemistry Definition Types Reactions and Applications

Organic Chemistry is one of the two branches of Chemistry. Thus forming an integral part of the subject. 


In this article, we will be learning about Organic Chemistry - What is Organic Chemistry will be discussed in the next section where the students will vividly understand the meaning of Organic Chemistry. We will also share the topics of organic chemistry that the students are required to understand. We will further our discussion, with the basic principles and techniques of organic chemistry in this context. 


Students are advised to go through the article in order to gain knowledge of Organic Chemistry.

Competitive Exams after 12th Science
tp-imag
bottom-arrow
tp-imag
bottom-arrow
tp-imag
bottom-arrow
tp-imag
bottom-arrow
tp-imag
bottom-arrow
tp-imag
bottom-arrow

What is Organic Chemistry?

Organic Chemistry is an integral part of Chemistry that studies organic compounds scientifically. Organic Compounds are those compounds containing covalently bonded carbon atoms. 


What do Organic Compounds Deal with?

Organic compounds deal with:

  • The structure of the Organic Compounds

  • Chemical Composition of Organic Compounds

  • Physical and Chemical Properties of Organic Compounds

  • Compounds undergoing the chemical processes 


Application of Organic Chemistry

Organic Chemistry has made some commendable contributions to the mankind:

  • Synthesis of several drugs, polymers, and other natural products

  • Design and construction of organic compounds for practical applications. 


Organic Chemistry Topics 

Check out the following contents which a student is required to study in Organic Chemistry. With the topics, we also have shared a brief explanation of the same so that the students understand the very gist of the concepts:

Serial No. 

Topics

Sub-topics


Structure and bonding

  • Dot structures: Structure and bonding

  • Hybridization: Structure and bonding

  • Bond-line structures



Resonance and acid-base chemistry

  • Counting electrons: Resonance and acid-base chemistry

  • Resonance structures: Resonance and acid-base chemistry

  • Organic acid-base chemistry



Alkanes, cycloalkanes, and functional groups

  • Naming alkanes: Alkanes, cycloalkanes, and functional groups

  • Naming alkanes, cycloalkanes, and bicyclic compounds: Alkanes, cycloalkanes, and functional groups

  • Conformations of alkanes: Alkanes, cycloalkanes, and functional groups

  • Conformations of cycloalkanes: Alkanes, cycloalkanes, and functional groups

  • Functional groups


Stereochemistry

  • Chirality: Stereochemistry

  • Enantiomers: Stereochemistry

  • Stereoisomeric relationships


Substitution and elimination reaction

  • Free radical reaction: Substitution and elimination reactions

  • Nucleophilicity and basicity: Substitution and elimination reactions

  • Elimination reactions: Substitution and elimination reactions

  • Sn1/Sn2/E1/E2: Substitution and elimination reactions

  • Sn1 and Sn2: Substitution and elimination reactions

  • E1 and E2 reactions: Substitution and elimination reactions

  • Sn1/Sn2/E1/E2


Alkenes and alkynes


  • Naming alkenes: Alkenes and alkynes

  • Alkene reactions: Alkenes and alkynes

  • Alkene nomenclature: Alkenes and alkynes

  • Alkene reactions: Alkenes and alkynes

  • Naming and preparing alkynes: Alkenes and alkynes

  • Alkyne reactions: Alkenes and alkynes

  • Synthesis using alkynes



Alcohols, ethers, epoxides, sulfides

  • Alcohol nomenclature and properties: Alcohols, ethers, epoxides, sulfides

  • Synthesis of alcohols: Alcohols, ethers, epoxides, sulfides

  • Reactions of alcohols: Alcohols, ethers, epoxides, sulfides

  • Nomenclature and properties of ethers: Alcohols, ethers, epoxides, sulfides

  • Synthesis and cleavage of ethers: Alcohols, ethers, epoxides, sulfides

  • Nomenclature and preparation of epoxides: Alcohols, ethers, epoxides, sulfides

  • Ring-opening reactions of epoxides: Alcohols, ethers, epoxides, sulfides

  • Thiols and sulfides



Conjugated systems and pericyclic reactions

Diels-Alder reaction


Aromatic compounds

  • Naming benzene derivatives: Aromatic compounds

  • Reactions of benzene: Aromatic compounds

  • Aromatic stability: Aromatic compounds

  • Electrophilic aromatic substitution: Aromatic compounds

  • Directing effects: Aromatic compounds

  • Other reactions and synthesis: Aromatic compounds

  • Nucleophilic aromatic substitution



Aldehydes and ketones

  • Introduction to aldehydes and ketones: Aldehydes and ketones

  • Reactions of aldehydes and ketones



Carboxylic acids and derivatives

  • Naming carboxylic acids: Carboxylic acids and derivatives

  • Formation of carboxylic acid derivatives: Carboxylic acids and derivatives

  • Nomenclature and reactions of carboxylic acids



Alpha carbon chemistry

Formation of enolate anions: Alpha carbon chemistry

Aldol condensations



Amines

Naming amines


Spectroscopy

  • Infrared spectroscopy: Spectroscopy

  • UV/Vis Spectroscopy: Spectroscopy

  • Proton NMR


Organic Chemistry - Some Basic Principles and Techniques 

In this section we will be studying Organic Chemistry Basics. Meaning we will have a brief discussion on the basic principles and techniques of Organic Chemistry. Study the following topics to know more about Organic Chemistry:

  1. Organic Chemistry - The Definition -

We have already studied the definition of Organic Chemistry which is the scientific study of carbon compounds, these carbon compounds are basically hydrocarbons and their derivatives. These compounds are extracted from plants and animals. 


  1. Carbon Shapes of the Organic Compounds - 

In this, we study catenation, which is defined as the atoms of an element that links to form chains and rings via itself and is thus known as the self-linking element. 

Further, in this topic, we also learn about ‘Tetravalency’ which means that the carbon compound is satisfied by forming the carbon, hydrogen, or other atoms.


  1. Structural Representation of Organic Compounds -

There are basically three structures of Organic Compounds formation:

  • Complete Structural Formula

  • Condensed Structural Formula

  • Bondline Structural Formula


  1. Classification of Organic Compounds - 

Organic Compounds can be classified into the following:

  • Acyclic or Open Chain Compounds & Alicyclic or Closed Chain or Ring Compounds

  • Aromatic Compounds

  • Heterocyclic Aromatic Compounds 


  1. Nomenclature of Organic Compounds - 

The nomenclature follows the suggestions of IUPAC in naming the organic compounds, carbocations, etc. 


  1. Methods of Purification of Organic Compounds -

Following are the methods of purification of organic compounds:

  • Simple crystallization 

  • Fractional crystallization 

  • Sublimation 

  • Simple distillation 

  • Fractional distillation

  • Steam distillation

  • Azeotropic distillation 

  • Chromatography 


Hope this article benefitted the students with required insights about Organic Chemistry. We have discussed the definition of Organic Compounds, the topics covered in the chapter of Organic Compounds, and the basic principles and bases of Organic Compounds

WhatsApp Banner

FAQs on Organic Chemistry Concepts Reactions and Mechanisms

1. What is organic chemistry?

Organic chemistry is the branch of chemistry that studies the structure, properties, reactions, and synthesis of carbon-containing compounds, especially those with C–H bonds. It focuses on compounds such as hydrocarbons, alcohols, acids, amines, and polymers.

  • Core element: Carbon (C)
  • Main bonding type: Covalent bonding
  • Applications: pharmaceuticals, plastics, fuels, biomolecules
Organic chemistry is essential for understanding life processes and industrial chemical production.

2. What are hydrocarbons in organic chemistry?

Hydrocarbons are organic compounds made only of carbon (C) and hydrogen (H) atoms. They are the simplest class of organic compounds and form the basis of petroleum and natural gas.

  • Alkanes: single bonds (e.g., CH4)
  • Alkenes: at least one C=C double bond (e.g., C2H4)
  • Alkynes: at least one C≡C triple bond (e.g., C2H2)
  • Aromatic hydrocarbons: benzene-type rings (e.g., C6H6)
Hydrocarbons undergo combustion, substitution, and addition reactions.

3. What is the difference between alkanes, alkenes, and alkynes?

The difference between alkanes, alkenes, and alkynes lies in the type of carbon–carbon bond present in the molecule.

  • Alkanes: only single C–C bonds; general formula CnH2n+2
  • Alkenes: at least one C=C double bond; general formula CnH2n
  • Alkynes: at least one C≡C triple bond; general formula CnH2n−2
Alkenes and alkynes are called unsaturated hydrocarbons because they can undergo addition reactions.

4. What is a functional group in organic chemistry?

A functional group is a specific atom or group of atoms in an organic molecule that determines its characteristic chemical reactions. Functional groups control physical properties, reactivity, and naming.

  • –OH: alcohol
  • –COOH: carboxylic acid
  • –NH2: amine
  • –CHO: aldehyde
Compounds with the same functional group show similar chemical behavior.

5. What is isomerism in organic chemistry?

Isomerism is the phenomenon where compounds have the same molecular formula but different structures or spatial arrangements. Isomers often have different physical and chemical properties.

  • Structural isomerism: different connectivity of atoms
  • Stereoisomerism: same connectivity but different 3D arrangement
Example: C4H10 has two structural isomers — n-butane and isobutane.

6. What is a homologous series?

A homologous series is a family of organic compounds with the same functional group and general formula, where consecutive members differ by a –CH2– unit. Members have similar chemical properties and gradual changes in physical properties.

  • Same functional group
  • Same general formula
  • Difference of 14 in molar mass (CH2)
Example: Alkanes — CH4, C2H6, C3H8.

7. What is the general formula for alkanes?

The general formula for alkanes is CnH2n+2, where n is the number of carbon atoms. This formula applies to open-chain saturated hydrocarbons.

  • n = 1 → CH4 (methane)
  • n = 2 → C2H6 (ethane)
  • n = 3 → C3H8 (propane)
Alkanes contain only single C–C and C–H bonds.

8. What is a substitution reaction in organic chemistry?

A substitution reaction is a reaction in which one atom or group in an organic molecule is replaced by another atom or group. It is common in alkanes and aromatic compounds.

  • Example (halogenation of methane):
CH4(g) + Cl2(g) → CH3Cl(g) + HCl(g)
  • Occurs in the presence of UV light
  • Typical of saturated hydrocarbons
Substitution reactions are important in preparing haloalkanes and other derivatives.

9. What is an addition reaction in organic chemistry?

An addition reaction is a reaction where atoms are added across a double or triple bond in an unsaturated organic compound. It is typical of alkenes and alkynes.

  • Example (hydrogenation of ethene):
C2H4(g) + H2(g) → C2H6(g)
  • Requires a Ni or Pt catalyst
  • Converts unsaturated compounds to saturated ones
Addition reactions reduce bond multiplicity.

10. What is combustion in organic chemistry?

Combustion in organic chemistry is the complete reaction of an organic compound with oxygen to produce CO2 and H2O, releasing heat. It is an exothermic oxidation reaction.

  • Example (combustion of methane):
CH4(g) + 2O2(g) → CO2(g) + 2H2O(l)
  • Produces energy
  • Used in fuels and engines
Incomplete combustion can produce CO instead of CO2.