Alkanes – Formula, Definition, Structure, Properties, List of Alkanes, Examples and FAQS

What are Alkanes?

Alkanes are organic compounds that consist of single-bonded carbon and hydrogen atoms. The formula for Alkanes is CnH2n+2, subdivided into three groups – chain alkanes, cycloalkanes, and the branched alkanes.

Alkane as saturated hydrocarbons

  • Alkanes are a series of compounds that contain carbon and hydrogen atoms with single covalent bonds. These are known as saturated hydrocarbons. This group of compounds consists of carbon and hydrogen atoms with single covalent bonds. Also comprises a homologous series having a molecular formula of CnH2n+2.
  • Alkanes are the simplest family of hydrocarbons. They contain only carbon and hydrogen. Each carbon atom forms four bonds and each hydrogen atom forms one bond. Chemists use line-angle formulas because they are easier and faster to draw than condensed structural formulas. Structural formulas for alkanes can be written in yet another condensed form.

The simple alkane methane contains one carbon atom and CH4 as its molecular formula. As this compound have just single covalent bonds only, therefore, its structural formula is

Alkanes are organic compounds that consist of single-bonded carbon and hydrogen atoms. The formula for Alkanes is CnH2n+2, subdivided into three groups – chain alkanes, cycloalkanes, and the branched alkanes.

In a long chain alkane molecule, additional carbon atoms are attached to each other with the help of a single covalent bond. Each atom is attached to the sufficient hydrogen atoms to develop a total of four single covalent bonds. This long-chain structure is known as octane. An eight-carbon alkane has a molecular formula – C 8H 18 and structural formula-

Alkanes are organic compounds that consist of single-bonded carbon and hydrogen atoms. The formula for Alkanes is CnH2n+2, subdivided into three groups – chain alkanes, cycloalkanes, and the branched alkanes.

List of Alkanes and its structures

The list of some Alkanes with the molecular formula and structures are given below.​

Physical Properties of Alkanes

1. The Solubility of Alkanes

  • Due to very little difference of electronegativity between carbon and hydrogen and covalent nature of C-C bond or C-H bond, alkanes are generally non-polar molecules.
  • As we generally observe, polar molecules are soluble in polar solvents whereas non-polar molecules are soluble in non-polar solvents. Hence, alkanes are hydrophobic in nature that is, alkanes are insoluble in water.
  • However, they are soluble in organic solvents as the energy required to overcome the existing Van Der Waals forces and generate new Van Der Waals forces is quite comparable.

2. The Boiling Point of Alkanes

  • As the intermolecular Van Der Waals forces increase with the increase of the molecular size or the surface area of the molecule we observe:
  • The boiling point of alkanes increases with increasing molecular weight,
  • The straight-chain alkanes are observed to have a higher boiling point in comparison to their structural isomers.

3. The Melting Point of Alkanes

  • The melting point of alkanes follow the same trend as their boiling point that is, it increases with increase in molecular weight.
  • This is attributed to the fact that higher alkanes are solids and it’s difficult to overcome intermolecular forces of attraction between them.
  • It is generally observed that even-numbered alkanes have a higher trend in melting point in comparison to odd-numbered alkanes as the even-numbered alkanes pack well in the solid phase, forming a well-organized structure which is difficult to break.

Also, Read in Detail: Physical & Chemical Properties of Alkanes

Alkanes Formula and its Condensed Structures

Structural formulas for alkanes can be written in condensed form. For example, the structural formula of pentane contains three CH2 methylene groups in the middle of the chain. We can group them together and write the structural formula. The first five alkanes formulas with an unbranched chain are tabulated below.

NameMolecular formula of alkaneCondensed structural formula of alkane
methaneCH4CH4
ethaneC2H6CH3CH3
propaneC3H8CH3CH2CH3
butaneC4H10CH3(CH2)2CH3
pentaneC5H12CH3(CH2)3CH3

An abbreviated way to draw structural formulas in which each vertex and line terminus represents a carbon atom and each line represents a bond.

Alkane Formula Chemistry

Formulas of organic compounds present information at several levels of sophistication. Molecular formulas, such as that of octane give the number of each kind of atom in a molecule of a compound. The molecular formula of C8H18 may apply to several alkanes, each one of which has unique chemical, physical and toxicological properties. These different compounds are designated by structural formulas showing the order in which the atoms in a molecule are arranged. Compounds that have the same molecular, but different structural formulas are called structural isomers.

Most organic compounds can be derived from alkanes. In addition, many important parts of organic molecules contain one or more alkane groups, minus a hydrogen atom, bonded as substituents onto the basic organic molecule. As a consequence of these factors, the names of many organic compounds are based on alkanes.

Branched Chain Alkane Formula

As with other organic compounds, the carbon atoms in alkanes may form straight chains, branched chains, or rings. These three kinds of alkanes are straight chain alkanes, branched chain alkanes and cycloalkanes. The general molecular formula of alkane for straight and branched-chain alkanes is CnH2n+2 and that of cyclic alkanes is CnH2n.

Alkanes are organic compounds that consist of single-bonded carbon and hydrogen atoms. The formula for Alkanes is CnH2n+2, subdivided into three groups – chain alkanes, cycloalkanes, and the branched alkanes.

For example in the diagram, the four hydrocarbon molecules contain 8 carbon atoms each. In one of the molecules, all the carbon atoms are in a straight chain and in two they are in branched chains, whereas in a fourth, 6 of the carbon atoms are in a ring.

Alkyl Groups

When a substituent like halogen bonds to an alkane molecule, one carbon-hydrogen bond of the molecule gets converted to a carbon-substituent bond. It can be understood with an example- A new compound known as chloromethane is formed when methane reacts with chlorine. The new compound is composed of a CH3 group that is bonded to a chlorine atom.

Alkanes are organic compounds that consist of single-bonded carbon and hydrogen atoms. The formula for Alkanes is CnH2n+2, subdivided into three groups – chain alkanes, cycloalkanes, and the branched alkanes.

When an alkane having hydrogen is removed from one bond, it is called an alkyl group. This Alkyl group is often denoted by the letter R the same as halogens represent by the letter X. Here is a methane‐chlorine reaction that can be generalized as

Alkanes are organic compounds that consist of single-bonded carbon and hydrogen atoms. The formula for Alkanes is CnH2n+2, subdivided into three groups – chain alkanes, cycloalkanes, and the branched alkanes.

Frequently Asked Questions – FAQs

Q1

What are the first four alkanes?

Methane (CH4), ethane (C2H6), propane (C3H8) and butane (C4H10) are the first four alkanes. Methane gas, whose molecular formula is CH4, is the simplest alkane.

Q2

How are alkanes classified?

Alkanes are single-bond hydrocarbon atoms. Three types of alkanes are available: linear straight alkanes branched alkanes and cyclic alkanes.

Q3

Is alkane a functional group?

Usually, alkanes are not considered functional groups; rather, an alkane is a compound that lacks functional groups. A carbon-carbon double bond is a functional group in an alkene.

Q4

What is the general formula of alkyne?

In a homologous series, alkynes are compounds with the general molecular formula of CnH2n‐2.

Q5

What is the simplest alkyne?

Alkynes are triple-bond carbon-carbon hydrocarbons. They do not display any geometric or optical isomerism. Ethyne (HC≡CH), frequently known as acetylene, is the easiest alkyne as shown on the right.

Er. Neeraj K.Anand is a freelance mentor and writer who specializes in Engineering & Science subjects. Neeraj Anand received a B.Tech degree in Electronics and Communication Engineering from N.I.T Warangal & M.Tech Post Graduation from IETE, New Delhi. He has over 30 years of teaching experience and serves as the Head of Department of ANAND CLASSES. He concentrated all his energy and experiences in academics and subsequently grew up as one of the best mentors in the country for students aspiring for success in competitive examinations. In parallel, he started a Technical Publication "ANAND TECHNICAL PUBLISHERS" in 2002 and Educational Newspaper "NATIONAL EDUCATION NEWS" in 2014 at Jalandhar. Now he is a Director of leading publication "ANAND TECHNICAL PUBLISHERS", "ANAND CLASSES" and "NATIONAL EDUCATION NEWS". He has published more than hundred books in the field of Physics, Mathematics, Computers and Information Technology. Besides this he has written many books to help students prepare for IIT-JEE and AIPMT entrance exams. He is an executive member of the IEEE (Institute of Electrical & Electronics Engineers. USA) and honorary member of many Indian scientific societies such as Institution of Electronics & Telecommunication Engineers, Aeronautical Society of India, Bioinformatics Institute of India, Institution of Engineers. He has got award from American Biographical Institute Board of International Research in the year 2005.

CBSE Class 11 Chemistry Syllabus

CBSE Class 11 Chemistry Syllabus is a vast which needs a clear understanding of the concepts and topics. Knowing CBSE Class 11 Chemistry syllabus helps students to understand the course structure of Chemistry.

Unit-wise CBSE Class 11 Syllabus for Chemistry

Below is a list of detailed information on each unit for Class 11 Students.

UNIT I – Some Basic Concepts of Chemistry

General Introduction: Importance and scope of Chemistry.

Nature of matter, laws of chemical combination, Dalton’s atomic theory: concept of elements,
atoms and molecules.

Atomic and molecular masses, mole concept and molar mass, percentage composition, empirical and molecular formula, chemical reactions, stoichiometry and calculations based on stoichiometry.

UNIT II – Structure of Atom

Discovery of Electron, Proton and Neutron, atomic number, isotopes and isobars. Thomson’s model and its limitations. Rutherford’s model and its limitations, Bohr’s model and its limitations, concept of shells and subshells, dual nature of matter and light, de Broglie’s relationship, Heisenberg uncertainty principle, concept of orbitals, quantum numbers, shapes of s, p and d orbitals, rules for filling electrons in orbitals – Aufbau principle, Pauli’s exclusion principle and Hund’s rule, electronic configuration of atoms, stability of half-filled and completely filled orbitals.

UNIT III – Classification of Elements and Periodicity in Properties

Significance of classification, brief history of the development of periodic table, modern periodic law and the present form of periodic table, periodic trends in properties of elements -atomic radii, ionic radii, inert gas radii, Ionization enthalpy, electron gain enthalpy, electronegativity, valency. Nomenclature of elements with atomic number greater than 100.

UNIT IV – Chemical Bonding and Molecular Structure

Valence electrons, ionic bond, covalent bond, bond parameters, Lewis structure, polar character of covalent bond, covalent character of ionic bond, valence bond theory, resonance, geometry of covalent molecules, VSEPR theory, concept of hybridization, involving s, p and d orbitals and shapes of some simple molecules, molecular orbital theory of homonuclear diatomic molecules(qualitative idea only), Hydrogen bond.

UNIT V – Chemical Thermodynamics

Concepts of System and types of systems, surroundings, work, heat, energy, extensive and intensive properties, state functions. First law of thermodynamics – internal energy and enthalpy, measurement of U and H, Hess’s law of constant heat summation, enthalpy of bond dissociation, combustion, formation, atomization, sublimation, phase transition, ionization, solution and dilution. Second law of Thermodynamics (brief introduction)
Introduction of entropy as a state function, Gibb’s energy change for spontaneous and nonspontaneous processes.
Third law of thermodynamics (brief introduction).

UNIT VI – Equilibrium

Equilibrium in physical and chemical processes, dynamic nature of equilibrium, law of mass action, equilibrium constant, factors affecting equilibrium – Le Chatelier’s principle, ionic equilibrium- ionization of acids and bases, strong and weak electrolytes, degree of ionization,
ionization of poly basic acids, acid strength, concept of pH, hydrolysis of salts (elementary idea), buffer solution, Henderson Equation, solubility product, common ion effect (with illustrative examples).

UNIT VII – Redox Reactions

Concept of oxidation and reduction, redox reactions, oxidation number, balancing redox reactions, in terms of loss and gain of electrons and change in oxidation number, applications of redox reactions.

UNIT VIII – Organic Chemistry: Some basic Principles and Techniques

General introduction, classification and IUPAC nomenclature of organic compounds. Electronic displacements in a covalent bond: inductive effect, electromeric effect, resonance and hyper conjugation. Homolytic and heterolytic fission of a covalent bond: free radicals, carbocations, carbanions, electrophiles and nucleophiles, types of organic reactions.

UNIT IX – Hydrocarbons

Classification of Hydrocarbons
Aliphatic Hydrocarbons:
Alkanes – Nomenclature, isomerism, conformation (ethane only), physical properties, chemical reactions.
Alkenes – Nomenclature, structure of double bond (ethene), geometrical isomerism, physical properties, methods of preparation, chemical reactions: addition of hydrogen, halogen, water, hydrogen halides (Markovnikov’s addition and peroxide effect), ozonolysis, oxidation, mechanism of electrophilic addition.
Alkynes – Nomenclature, structure of triple bond (ethyne), physical properties, methods of preparation, chemical reactions: acidic character of alkynes, addition reaction of – hydrogen, halogens, hydrogen halides and water.

Aromatic Hydrocarbons:

Introduction, IUPAC nomenclature, benzene: resonance, aromaticity, chemical properties: mechanism of electrophilic substitution. Nitration, sulphonation, halogenation, Friedel Craft’s alkylation and acylation, directive influence of functional group in monosubstituted benzene. Carcinogenicity and toxicity.

To know the CBSE Syllabus for all the classes from 1 to 12, visit the Syllabus page of CBSE. Meanwhile, to get the Practical Syllabus of Class 11 Chemistry, read on to find out more about the syllabus and related information in this page.

CBSE Class 11 Chemistry Practical Syllabus with Marking Scheme

In Chemistry subject, practical also plays a vital role in improving their academic scores in the subject. The overall weightage of Chemistry practical mentioned in the CBSE Class 11 Chemistry syllabus is 30 marks. So, students must try their best to score well in practicals along with theory. It will help in increasing their overall academic score.

CBSE Class 11 Chemistry Practical Syllabus

The experiments will be conducted under the supervision of subject teacher. CBSE Chemistry Practicals is for 30 marks. This contribute to the overall practical marks for the subject.

The table below consists of evaluation scheme of practical exams.

Evaluation SchemeMarks
Volumetric Analysis08
Salt Analysis08
Content Based Experiment06
Project Work04
Class record and viva04
Total30

CBSE Syllabus for Class 11 Chemistry Practical

Micro-chemical methods are available for several of the practical experiments. Wherever possible such techniques should be used.

A. Basic Laboratory Techniques
1. Cutting glass tube and glass rod
2. Bending a glass tube
3. Drawing out a glass jet
4. Boring a cork

B. Characterization and Purification of Chemical Substances
1. Determination of melting point of an organic compound.
2. Determination of boiling point of an organic compound.
3. Crystallization of impure sample of any one of the following: Alum, Copper Sulphate, Benzoic Acid.

C. Experiments based on pH

1. Any one of the following experiments:

  • Determination of pH of some solutions obtained from fruit juices, solution of known and varied concentrations of acids, bases and salts using pH paper or universal indicator.
  • Comparing the pH of solutions of strong and weak acids of same concentration.
  • Study the pH change in the titration of a strong base using universal indicator.

2. Study the pH change by common-ion in case of weak acids and weak bases.

D. Chemical Equilibrium
One of the following experiments:

1. Study the shift in equilibrium between ferric ions and thiocyanate ions by increasing/decreasing the concentration of either of the ions.
2. Study the shift in equilibrium between [Co(H2O)6] 2+ and chloride ions by changing the concentration of either of the ions.

E. Quantitative Estimation
i. Using a mechanical balance/electronic balance.
ii. Preparation of standard solution of Oxalic acid.
iii. Determination of strength of a given solution of Sodium hydroxide by titrating it against standard solution of Oxalic acid.
iv. Preparation of standard solution of Sodium carbonate.
v. Determination of strength of a given solution of hydrochloric acid by titrating it against standard Sodium Carbonatesolution.

F. Qualitative Analysis
1) Determination of one anion and one cation in a given salt
Cations‐ Pb2+, Cu2+, As3+, Al3+, Fe3+, Mn2+, Ni2+, Zn2+, Co2+, Ca2+, Sr2+, Ba2+, Mg2+, NH4 +
Anions – (CO3)2‐ , S2‐, NO2 , SO32‐, SO2‐ , NO , Cl , Br, I‐, PO43‐ , C2O2‐ ,CH3COO
(Note: Insoluble salts excluded)

2) Detection of ‐ Nitrogen, Sulphur, Chlorine in organic compounds.

G) PROJECTS
Scientific investigations involving laboratory testing and collecting information from other sources.

A few suggested projects are as follows:

  • Checking the bacterial contamination in drinking water by testing sulphide ion
  • Study of the methods of purification of water.
  • Testing the hardness, presence of Iron, Fluoride, Chloride, etc., depending upon the regional
    variation in drinking water and study of causes of presence of these ions above permissible
    limit (if any).
  • Investigation of the foaming capacity of different washing soaps and the effect of addition of
    Sodium carbonate on it.
  • Study the acidity of different samples of tea leaves.
  • Determination of the rate of evaporation of different liquids Study the effect of acids and
    bases on the tensile strength of fibres.
  • Study of acidity of fruit and vegetable juices.

Note: Any other investigatory project, which involves about 10 periods of work, can be chosen with the approval of the teacher.

Practical Examination for Visually Impaired Students of Class 11

Below is a list of practicals for the visually impaired students.

A. List of apparatus for identification for assessment in practicals (All experiments)
Beaker, tripod stand, wire gauze, glass rod, funnel, filter paper, Bunsen burner, test tube, test tube stand,
dropper, test tube holder, ignition tube, china dish, tongs, standard flask, pipette, burette, conical flask, clamp
stand, dropper, wash bottle
• Odour detection in qualitative analysis
• Procedure/Setup of the apparatus

B. List of Experiments A. Characterization and Purification of Chemical Substances
1. Crystallization of an impure sample of any one of the following: copper sulphate, benzoic acid
B. Experiments based on pH
1. Determination of pH of some solutions obtained from fruit juices, solutions of known and varied
concentrations of acids, bases and salts using pH paper
2. Comparing the pH of solutions of strong and weak acids of same concentration.

C. Chemical Equilibrium
1. Study the shift in equilibrium between ferric ions and thiocyanate ions by increasing/decreasing
the concentration of eitherions.
2. Study the shift in equilibrium between [Co(H2O)6]2+ and chloride ions by changing the
concentration of either of the ions.

D. Quantitative estimation
1. Preparation of standard solution of oxalic acid.
2. Determination of molarity of a given solution of sodium hydroxide by titrating it against standard
solution of oxalic acid.

E. Qualitative Analysis
1. Determination of one anion and one cation in a given salt
2. Cations – NH+4
Anions – (CO3)2-, S2-, (SO3)2-, Cl-, CH3COO-
(Note: insoluble salts excluded)
3. Detection of Nitrogen in the given organic compound.
4. Detection of Halogen in the given organic compound.

Note: The above practicals may be carried out in an experiential manner rather than recording observations.

We hope students must have found this information on CBSE Syllabus useful for their studying Chemistry. Learn Maths & Science in interactive and fun loving ways with ANAND CLASSES (A School Of Competitions) App/Tablet.

Frequently Asked Questions on CBSE Class 11 Chemistry Syllabus

Q1

How many units are in the CBSE Class 11 Chemistry Syllabus?

There are 9 units in the CBSE Class 11 Chemistry Syllabus. Students can access various study materials for the chapters mentioned in this article for free at ANAND CLASSES (A School Of Competitions).

Q2

What is the total marks for practicals examination as per the CBSE Class 11 Chemistry Syllabus?

The total marks for the practicals as per the CBSE Class 11 Chemistry Syllabus is 30. It includes volumetric analysis, content-based experiment, salt analysis, class record, project work and viva.

Q3

Which chapter carries more weightage as per the CBSE Syllabus for Class 11 Chemistry?

The organic chemistry chapter carries more weightage as per the CBSE Syllabus for Class 11 Chemistry.