Solutions for Chapter 2.21: Chemical Properties: Combustion of Alkanes

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 2.21: Chemical Properties: Combustion of Alkanes

Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2.21: Chemical Properties: Combustion of Alkanes includes 4 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 4 problems in chapter 2.21: Chemical Properties: Combustion of Alkanes have been answered, more than 10850 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acetylide ion

    The conjugate base of acetylene or any terminal alkyne.

  • Amino group

    A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms

  • amplitude.

    The vertical distance from the middle of a wave to the peak or trough. (7.1)

  • Arrhenius equation

    An equation that relates the rate constant for a reaction to the frequency factor, A, the activation energy, Ea, and the temperature, T: k = Ae-Ea>RT. In its logarithmic form it is written ln k = -Ea>RT + ln A. (Section 14.5)

  • buffer solution.

    A solution of (a) a weak acid or base and (b) its salt; both components must be present. The solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. (16.3)

  • concentration cell

    A voltaic cell containing the same electrolyte and the same electrode materials in both the anode and cathode compartments. The emf of the cell is derived from a difference in the concentrations of the same electrolyte solutions in the compartments. (Section 20.6)

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • diastereotopic

    Nonequivalent protons for which the replacement test produces diastereomers.

  • Dihedral angle

    The angle created by two intersecting planes.

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • half-reaction

    An equation for either an oxidation or a reduction that explicitly shows the electrons involved, for example, Zn2 + 1aq2 + 2 e- ยก Zn1s2. (Section 20.2)

  • heterocycle

    A cyclic compound containing at least one heteroatom (such as S, N, or O) in the ring.

  • hydrogen bonding

    Bonding that results from intermolecular attractions between molecules containing hydrogen bonded to an electronegative element. The most important examples involve OH, NH, and HF. (Section 11.2)

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • metallic hydrides

    Compounds formed when hydrogen reacts with transition metals; these compounds contain the hydride ion, H-. (Section 22.2)

  • molecularity

    The number of molecules that participate as reactants in an elementary reaction. (Section 14.6)

  • neutron

    An electrically neutral particle found in the nucleus of an atom; it has approximately the same mass as a proton. (Section 2.3)

  • peptide bond

    The amide linkage by which two amino acids are coupled together to form peptides.

  • Thermoplastic

    A polymer that can be melted and molded into a shape that is retained when it is cooled.

  • Wittig reaction

    A reaction that converts an aldehyde or ketone into an alkene, with the introduction of one or more carbon atoms.

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