Solutions for Chapter 3.10: Conformational Analysis of Monosubstituted Cyclohexanes

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 3.10: Conformational Analysis of Monosubstituted Cyclohexanes

Solutions for Chapter 3.10
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Chapter 3.10: Conformational Analysis of Monosubstituted Cyclohexanes includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 3.10: Conformational Analysis of Monosubstituted Cyclohexanes have been answered, more than 8589 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • aldonic acid

    The product obtained when the aldehyde group of an aldose is oxidized.

  • angstrom

    A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)

  • binary compounds.

    Compounds formed from just two elements. (2.7)

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • common-ion effect

    A shift of an equilibrium induced by an ion common to the equilibrium. For example, added Na2SO4 decreases the solubility of the slightly soluble salt BaSO4, or added NaF decreases the percent ionization of HF. (Section 17.1)

  • degenerate orbitals

    Orbitals that have the same energy.

  • deoxyribonucleic acids (DNA).

    A type of nucleic acid. (25.4)

  • dihedral angle

    The angle by which two groups are separated in a Newman projection.

  • ether

    A compound with the structure R!O!R.

  • face-centered lattice

    A crystal lattice in which the lattice points are located at the faces and corners of each unit cell. (Section 12.2)

  • hybridization

    The mixing of different types of atomic orbitals to produce a set of equivalent hybrid orbitals. (Section 9.5)

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • hydrophobic

    Water repelling. The term is often used to describe a type of colloid. (Section 13.6)

  • ionic bond

    A bond that results from the force of attraction between two oppositely charged ions.

  • molecular equation

    A chemical equation in which the formula for each substance is written without regard for whether it is an electrolyte or a nonelectrolyte. (Section 4.2)

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • para

    On an aromatic ring, the C4position.

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • pressure–volume (PV) work

    Work performed by expansion of a gas against a resisting pressure. (Section 5.3)

  • single bond

    A covalent bond involving one electron pair. (Section 8.3)

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