Solutions for Chapter 2.T: Organic Chemistry 7th Edition

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781269406772

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 2.T

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 13 problems in chapter 2.T have been answered, more than 89727 students have viewed full step-by-step solutions from this chapter. Chapter 2.T includes 13 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Sieva Kozinsky and is associated to the ISBN: 9781269406772.

Key Chemistry Terms and definitions covered in this textbook
  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • addition reactions

    Reactions that are characterized by the addition of two groups across a double bond. In the process, the pi (p) bond is broken.

  • alpha (a) position

    The position immediately adjacent to a functional group.

  • autocatalytic

    A reaction for which the reagent necessary to catalyze the reaction is produced by the reaction itself.

  • bidentate ligand

    A ligand in which two linked coordinating atoms are bound to a metal. (Section 23.3)

  • Chromatography

    A separation method involving passing a vapor or solution mixture through a column packed with a material with different affi nities for different components of the mixture.

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • Diels-Alder adduct

    A cyclohexene resulting from the cycloaddition reaction of a diene and a dienophile.

  • dihedral angle

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

  • fuel value

    The energy released when 1 g of a substance is combusted. (Section 5.8)

  • Heterocyclic aromatic amine

    An amine in which nitrogen is one of the atoms of an aromatic ring.

  • high-resolution mass spectrometry

    A technique that involves the use of a detector that can measure the m/z values to four decimal places.This technique allows for the determination of the molecular formula of an unknown compound.

  • 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

  • hydration

    Solvation when the solvent is water. (Section 13.1)

  • hydrochlorofluorocarbons, (HCFCs)

    Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.

  • Photodynamic therapy

    Biological damage caused by photosensitizers, light, and oxygen, used to kill tumor and other cells.

  • pressure–volume (PV) work

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

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

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