×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 10.8: Bonding in Allenes

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 10.8: Bonding in Allenes

Solutions for Chapter 10.8
4 5 0 373 Reviews
25
4

This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 1 problems in chapter 10.8: Bonding in Allenes have been answered, more than 36556 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 10.8: Bonding in Allenes includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • absorption spectrum

    In IR spectroscopy as well as UV-VIS spectroscopy, a plot that measures the percent transmittance or absorption as a function of frequency.

  • alkane

    A hydrocarbon that lacks p bonds.

  • atomic radius.

    One-half the distance between the two nuclei in two adjacent atoms of the same element in a metal. For elements that exist as diatomic units, the atomic radius is one-half the distance between the nuclei of the two atoms in a particular molecule. (8.3)

  • continuous-wave (CW) spectrometer

    An NMR spectrometer that holds the magnetic field constant and slowly sweeps through a range of rf frequencies, monitoring which frequencies are absorbed.

  • dipole moment

    A measure of the separation and magnitude of the positive and negative charges in polar molecules. (Section 8.4)

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • 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)

  • microstate

    The state of a system at a particular instant; one of many possible energetically equivalent ways to arrange the components of a system to achieve a particular state. (Section 19.3)

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • oligomers

    During the polymerization process, compounds constructed from just a few monomers.

  • polarizability

    The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • symmetric stretching

    In IR spectroscopy, when two bonds are stretching in phase with each other.

  • Telechelic polymer

    A polymer in which its growing chains are terminated by formation of new functional groups at both ends of its chains. These new functional groups are introduced by adding reagents, such as CO2 or ethylene oxide, to the growing chains.

  • termination

    In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password