Careers360 Logo
ask-icon
share
    JEE Main 2026 April 7 Paper 2 Answer Key (Out) - Download PDF

    Conformation, Sawhorse and Newman Projections - Practice Questions & MCQ

    Edited By admin | Updated on Sep 18, 2023 18:35 AM | #JEE Main

    Quick Facts

    • 16 Questions around this concept.

    Solve by difficulty

    In the following structures, which one is having staggered conformation with maximum dihedral angle?

    Arrange the following conformational isomers of n-butane in order of their increasing potential energy :

    Which one of the following conformer of butane is most stable ? 

    In the given conformation $C_2$ is rotated about $C_2-C_3$ bond anticlockwise by an angle of $120^{\circ}$ then the formation obtained is

    In the following the most stable conformation of n-butane is:

    The incorrect statement regarding conformations of ethane is :

    Newman projection P, Q, R and S are shown below. Which one of the following represent identical molecule?

    Amity University Noida-B.Tech Admissions 2026

    Among top 100 Universities Globally in the Times Higher Education (THE) Interdisciplinary Science Rankings 2026

    UPES B.Tech Admissions 2026

    Last Date to Apply: 29th April | Ranked #43 among Engineering colleges in India by NIRF | Highest Package 1.3 CR , 100% Placements

    The most stable conformation for n-butane is

    The most stable conformation of 2,3 -dibromobutane is

    JEE Main 2026 College Predictor
    Check your college admission chances based on your JEE Main percentile with the JEE Main 2026 College Predictor.
    Try Now

    Which one of the following conformations of cyclohexane is chiral?

    Concepts Covered - 1

    Conformation, Sawhorse and Newman Projections

    Conformations
    Alkanes contain carbon-carbon sigma (σ) bonds. Electron distribution of the sigma molecular orbital is symmetrical around the internuclear axis of the C–C bond which is not disturbed due to rotation about its axis. This permits free rotation about C–C single bond. This rotation results into different spatial arrangements of atoms in space which can change into one another. Such spatial arrangements of atoms which can be converted into one another by rotation around a C-C single bond are called conformations or conformers or rotamers. Alkanes can thus have infinite number of conformations by rotation around C-C single bonds. However, it may be remembered that rotation around a C-C single bond is not completely free. It is hindered by a small energy barrier of 1-20 kJ mol–1 due to weak repulsive interaction between the adjacent bonds. Such a type of repulsive interaction is called torsional strain.

    Sawhorse projections
    In this projection, the molecule is viewed along the molecular axis. It is then projected on paper by drawing the central C–C bond as a somewhat longer straight line. Upper end of the line is slightly tilted towards right or left hand side. The front carbon is shown at the lower end of the line, whereas the rear carbon is shown at the upper end. Each carbon has three lines attached to it corresponding to three hydrogen atoms. The lines are inclined at an angle of 120° to each other. Sawhorse projections of eclipsed and staggered conformations of ethane are shown in the figure.

    Newman projections
    In this projection, the molecule is viewed at the C–C bond head on. The carbon atom nearer to the eye is represented by a point. Three hydrogen atoms attached to the front carbon atom are shown by three lines drawn at an angle of 120° to each other. The rear carbon atom is represented by a circle and the three hydrogen atoms are shown attached to it by the shorter lines drawn at an angle of 120° to each other. The Newman’s projections for ethane are shown in the figure.

    Study it with Videos

    Conformation, Sawhorse and Newman Projections

    "Stay in the loop. Receive exam news, study resources, and expert advice!"

    Books

    Reference Books

    Conformation, Sawhorse and Newman Projections

    Chemistry Part II Textbook for Class XI

    Page No. : 383

    Line : 1

    E-books & Sample Papers

    Get Answer to all your questions