

Organic Chemistry Some Basic Principles and Techniques Class 11
Chemistry for class 11 has this chapter named Organic Chemistry- Some Basic Principles and Techniques and it is very crucial for the students to score well in their examinations. Understanding the basics of organic chemistry will help them comprehend all the topics associated with it. In this article, we will cover some basic principles and techniques of Organic Chemistry in the simplest manner making it interesting.
Many entrance examinations such as IIT, NEET and other state board entrance tests will have MCQs on this chapter and all the students will get answers to the important questions after going through the organic chemistry some basic principles and techniques notes class 11 provided here.
What is Organic Chemistry?
Organic Chemistry is a subset of chemistry dealing with compounds of carbon. Therefore, we can say that Organic chemistry is the chemistry of carbon compounds and is 200-225 years old. Carbon forms bonds with itself to form long chains of hydrocarbons, e.g.CH4, methane and CH3-CH3 ethane. Carbon has the ability to form carbon-carbon bonds quite elaborately. Polymers like polyethylene is a linear chain where hundreds of CH2 are linked together.
Carbon can form bonds with other elements of the periodic table such as with H, N, S, O, P and halogens. The compounds formed will also be called organic compounds.
Lipids, DNA, proteins and carbohydrates also belong to the category of organic compounds which are essential for the sustenance of lives.
Vital Force Theory- It was proposed by the Swedish scientist named Berzelius in the year 1780. According to this theory, if you want to make an organic compound, you need to have a living system like a plant or animal. As earlier organic molecules were typically isolated from nature, plant material or animals or any other living organisms, this theory was believed to be in existence for several decades.
Organic Synthesis
(Making Organic compounds in the laboratory)
Later in the year 1828, another scientist named Frederich Wohler who performed a path-breaking experiment to disprove this theory which stated that living organisms are necessary to produce organic compounds.
The experiment included mixing NH4Cl + KCNO to get NH4CNO and upon heating the resulting compound, Urea was obtained. Urea is the first laboratory synthesized organic compound. This proved that there is no necessity of living organisms to synthesize organic compounds.
In 1885, Kolbe was involved in the synthesis of acetic acid (CH3COOH) also known as vinegar in the laboratory.
In 1856, Berthelot experimented to synthesise methane (CH4) from Aluminium Carbide (Al4C3) after undergoing hydrolysis.
Importance of Organic Chemistry
Organic chemistry is applicable in a variety of areas including-
Medicines: Example- Aspirin which is a headache medicine and Ibuprofen is a painkiller, both are organic compounds. Other examples include paracetamol.
Food: Example- Starch which is a carbohydrate is an organic compound and a constituent of rice and other grains. It is the source of energy.
Clothing: Example- Nylon, Polyester and Cotton are forms of organic compounds.
Fuels: Examples- Gasoline, Petrol and Diesel are organic compounds used in the automobile industry at large.
Shapes of Organic Molecules
Organic molecules may be three dimensional (3D), two dimensional (2D) or one dimensional, depending upon the kind of carbon we are dealing with.
As we already know that tetravalence of carbon and the formation of covalent bonds by it are talked in terms of its electronic configuration and the hybridisation of s and p orbitals. It can also be recalled that formation and the shapes of different molecules like methane (CH4), ethene (C2H4) and ethyne (C2H2) can be well explained in terms of the use of sp3, sp2 and sp hybrid orbitals by carbon atoms in the respective molecules.
Hybridisation influences the bond length and bond enthalpy, also known as its strength in organic compounds. The sp hybrid orbital consists of more s character and hence it is closer to its nucleus; it forms stronger and shorter bonds than the sp3 hybrid orbital. The sp2 hybrid orbital is intermediate in s character, usually between sp and sp3 and,therefore, the length and enthalpy of the bonds it forms, are also intermediate between them.
The alteration in hybridisation affects the electronegativity of carbon. The more the s character of the hybrid orbitals, the more is the electronegativity. Thus, a carbon atom with an sp hybrid orbital with 50% s character has higher electronegativity than that possessing sp2 or sp3 hybridised orbitals. This relative electronegativity is reflected in various physical and chemical properties of the molecules concerned. It will be covered in later chapters of Chemistry.
Further, NCERT books for Chemistry has covered many other topics such as classification of organic compounds, naming the compounds according to the IUPAC system of nomenclature, derivation of structures from their names, types of organic reactions, techniques of purification of organic compounds, etc.
Students can add a few more sub topics from organic chemistry, some basic principles and techniques, notes from class 11 NCERT books. Also, they can refer to our NCERT solutions for the problems associated with this chapter.
FAQs on Organic Chemistry- Some Basic Principles and Techniques
1. What key concepts are covered in the Class 11 chapter 'Organic Chemistry: Some Basic Principles and Techniques'?
This foundational chapter, often called General Organic Chemistry (GOC), introduces the core principles that govern organic molecules. As per the CBSE 2025-26 syllabus, key concepts include:
- Structure of Carbon: Understanding the tetravalency of carbon and shapes of organic molecules based on sp, sp², and sp³ hybridisation.
- Classification & Nomenclature: Systematically classifying and naming organic compounds using the IUPAC system.
- Reaction Mechanisms: Learning about electronic effects like the inductive effect and resonance, how covalent bonds break (homolytic and heterolytic cleavage), and the reactive species formed (carbocations, carbanions, free radicals).
- Purification Techniques: Methods for purifying organic compounds, such as crystallisation, distillation, and chromatography.
2. Which chapter is commonly known as General Organic Chemistry (GOC) in the CBSE Class 11 syllabus?
The chapter titled 'Organic Chemistry: Some Basic Principles and Techniques' is widely referred to as General Organic Chemistry (GOC) by students and teachers. It's given this name because it establishes the fundamental rules, concepts, and mechanisms—like nomenclature, isomerism, and electronic effects—that are essential for understanding all subsequent chapters on organic chemistry in both Class 11 and Class 12.
3. Why is understanding the hybridisation of carbon (sp, sp², sp³) so important in organic chemistry?
Understanding carbon's hybridisation is critical because it directly determines the properties of an organic molecule. It influences:
- Molecular Geometry: sp³ hybridisation leads to a tetrahedral shape (e.g., methane), sp² to a trigonal planar shape (e.g., ethene), and sp to a linear shape (e.g., ethyne).
- Bond Characteristics: As the s-character increases from sp³ to sp, the bonds become shorter, stronger, and the carbon atom becomes more electronegative.
- Reactivity: The shape and bond strength dictated by hybridisation play a crucial role in how a molecule will react with other substances.
4. What is the fundamental difference between an electrophile and a nucleophile?
The fundamental difference lies in their relationship with electrons. An electrophile (electron-loving) is an electron-deficient species that seeks electrons to complete its octet. It is typically a positive ion (like H⁺) or a neutral molecule with an electron-deficient centre (like AlCl₃). A nucleophile (nucleus-loving) is an electron-rich species that donates an electron pair to form a new covalent bond. It is often a negative ion (like OH⁻) or a neutral molecule with a lone pair of electrons (like NH₃).
5. How is a carbocation formed, and why is its stability a critical factor in organic reactions?
A carbocation is a positively charged carbon atom formed through the heterolytic cleavage of a covalent bond, where the leaving group takes both bonding electrons. Its stability is critical because most organic reactions proceed through the most stable possible intermediate. The stability order is Tertiary (3°) > Secondary (2°) > Primary (1°). This stability is influenced by:
- Inductive Effect: Alkyl groups donate electron density, which helps disperse the positive charge.
- Hyperconjugation: The delocalisation of sigma electrons from adjacent C-H bonds also helps stabilise the positive charge.
6. What is the main purpose of using the IUPAC nomenclature system in organic chemistry?
The main purpose of the IUPAC (International Union of Pure and Applied Chemistry) nomenclature system is to provide a logical and systematic set of rules for naming organic compounds. This ensures that every compound has a unique and unambiguous name that reveals its chemical structure. It eliminates the confusion caused by common or trivial names (like 'acetic acid' for ethanoic acid), allowing chemists worldwide to communicate with clarity and precision.
7. How does homolytic cleavage differ from heterolytic cleavage?
Homolytic and heterolytic cleavage are two ways a covalent bond can break:
- Homolytic Cleavage: The bond breaks symmetrically, with each atom retaining one of the bonding electrons. This process results in the formation of highly reactive, neutral species called free radicals. It is typically initiated by heat or UV light.
- Heterolytic Cleavage: The bond breaks asymmetrically, with one atom taking both bonding electrons. This results in the formation of charged species, or ions (a cation and an anion). This type of cleavage is more common in polar solvents.
8. What are electronic displacement effects, and why are they important?
Electronic displacement effects describe the shifting of electrons within a molecule, which creates centres of high or low electron density. This is crucial for determining a molecule's reactivity. The main types are:
- Inductive Effect: A permanent effect involving the shifting of sigma (σ) electrons due to the electronegativity difference between bonded atoms.
- Resonance (Mesomeric Effect): The delocalisation of pi (π) electrons across a conjugated system, leading to multiple contributing structures.
- Hyperconjugation: The delocalisation of sigma (σ) electrons of a C-H bond into an adjacent empty or partially filled orbital.

















