Solutions for Chapter 3.13: Conformers of Cyclohexane

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 3.13: Conformers of Cyclohexane

Solutions for Chapter 3.13
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This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Since 1 problems in chapter 3.13: Conformers of Cyclohexane have been answered, more than 15111 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780134042282. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3.13: Conformers of Cyclohexane includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • actual yield.

    The amount of product actually obtained in a reaction. (3.10)

  • atomic mass.

    The mass of an atom in atomic mass units. (3.1)

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • Brønsted–Lowry acid

    A substance (molecule or ion) that acts as a proton donor. (Section 16.2)

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • force

    A push or a pull. (Section 5.1)

  • Frost circles

    A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.

  • Lewis structure

    A representation of covalent bonding in a molecule that is drawn using Lewis symbols. Shared electron pairs are shown as lines, and unshared electron pairs are shown as pairs of dots. Only the valence-shell electrons are shown. (Section 8.3)

  • metric system

    A system of measurement used in science and in most countries. The meter and the gram are examples of metric units. (Section 1.4)

  • ortho

    On an aromatic ring, the C2 position.

  • oxidation

    A reaction in which one compound undergoes an increase in oxidation state.

  • Polarizability

    A measure of the ease of distortion of the distribution of electron density about an atom or group in response to interaction with other molecules or ions. Fluorine which has a high electronegativity and holds its electrons tightly, has a very low polarizability. Iodine, which has a lower electronegativity and holds its electrons less tightly, has a very high polarizability.

  • property

    A characteristic that gives a sample of matter its unique identity. (Section 1.1)

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • root-mean-square (rms) speed 1M2

    The square root of the average of the squared speeds of the gas molecules in a gas sample. (Section 10.7)

  • salt

    An ionic compound formed by replacing one or more hydrogens of an acid by other cations. (Section 4.3)

  • significant figures

    The digits that indicate the precision with which a measurement is made; all digits of a measured quantity are significant, including the last digit, which is uncertain. (Section 1.5)

  • termolecular

    For mechanisms, a step that involves three chemical entities.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.

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