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Solutions for Chapter Lesson 82: Preparing Solutions

Full solutions for Living by Chemistry | 2nd Edition

ISBN: 9781464142314

Solutions for Chapter Lesson 82: Preparing Solutions

This expansive textbook survival guide covers the following chapters and their solutions. Living by Chemistry was written by and is associated to the ISBN: 9781464142314. This textbook survival guide was created for the textbook: Living by Chemistry, edition: 2. Chapter Lesson 82: Preparing Solutions includes 8 full step-by-step solutions. Since 8 problems in chapter Lesson 82: Preparing Solutions have been answered, more than 24628 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Achiral

    An object that lacks chirality; an object that has no handedness

  • activated complex (transition state)

    The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)

  • annulenes

    Compounds consisting of a single ring containing a fully conjugated p system. Benzene is [6]annulene.

  • Bond dipole moment

    A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms

  • Bredt’s rule

    A rule that states that it is not possible for a bridgehead carbon of a bicyclic system to possess a carbon carbon double bond if it involves a trans p bond being incorporated in a ring comprised of fewer than eight atoms.

  • Cis, trans isomers

    Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • crossed aldol reaction

    An aldol reaction that occurs between different partners.

  • downfield

    The left side of an NMR spectrum.

  • E2

    A bimolecular b-elimination reaction.

  • empirical formula

    A chemical formula that shows the kinds of atoms and their relative numbers in a substance in the smallest possible whole-number ratios. (Section 2.6)

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Haber process

    The catalyst system and conditions of temperature and pressure developed by Fritz Haber and coworkers for the formation of NH3 from H2 and N2. (Section 15.2)

  • heat of vaporization

    The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)

  • integration

    In 1H NMR spectroscopy, the area under a signal indicates the number of protons giving rise to the signal.

  • l-Monosaccharide

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

  • Lewis base

    A compound capable offunctioning as an electron pair donor.

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

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