×
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 8.6SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 8.6SE

Solutions for Chapter 8.6SE
4 5 0 369 Reviews
20
0

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 8.6SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 8.6SE have been answered, more than 174968 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alpha (a) amino acid

    A compound containing a carboxylic acid group (COOH) as well as an amino group (NH2), both of which are attached to the same carbon atom.

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • Brønsted base.

    A substance capable of accepting a proton. (4.3)

  • catalyst

    A compound that can speed up the rate of a reaction without itself being consumed by the reaction.

  • complex ion (complex)

    An assembly of a metal ion and the Lewis bases (ligands) bonded to it. (Section 17.5)

  • condensation reaction

    A chemical reaction in which a small molecule (such as a molecule of water) is split out from between two reacting molecules. (Sections 12.6 and 22.8)

  • degenerate

    A situation in which two or more orbitals have the same energy. (Section 6.7)

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • Diels-Alder adduct

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

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • elimination (of radicals)

    In radical reaction mechanisms, a step in which a bond forms between the alpha (a) and beta (b) positions. As a result, a single bond at the b position is cleaved, causing the compound to fragment into two pieces.

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • excited state

    A state that is achieved when a compound absorbs energy.

  • Gauche conformation

    A conformation about a single bond of an alkane in which two groups on adjacent carbons lie at a dihedral angle of 60°

  • Low-density lipoprotein (LDL)

    Plasma particles, density 1.02–1.06 g/mL, consisting of approximately 26% proteins, 50% cholesterol, 21% phospholipids, and 4% triglycerides.

  • Michael donor

    The nucleophile in a Michael reaction.

  • representative (main-group) element

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

  • s-trans

    A conformation of a conjugateddiene in which the disposition of the two p bonds with regard to the connecting single bond is translike (a dihedral angle of 180°).

  • Steric strain

    The strain that arises when nonbonded atoms separated by four or more bonds are forced closer to each other than their atomic (contact) radii would allow. Steric strain is also called non-bonded interaction strain, or van der Waals strain.

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

×
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