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Solutions for Chapter Chapter 23: Chemical Equilibrium

Full solutions for Living by Chemistry | 2nd Edition

ISBN: 9781464142314

Solutions for Chapter Chapter 23: Chemical Equilibrium

Since 4 problems in chapter Chapter 23: Chemical Equilibrium have been answered, more than 23455 students have viewed full step-by-step solutions from this chapter. Chapter Chapter 23: Chemical Equilibrium includes 4 full step-by-step solutions. This textbook survival guide was created for the textbook: Living by Chemistry, edition: 2. Living by Chemistry was written by and is associated to the ISBN: 9781464142314. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • (n 1 1) rule

    If a hydrogen has n hydrogens nonequivalent to it but equivalent among themselves on the same or adjacent atom(s), its 1 H!NMR signal is split into (n 1 1) peaks

  • amine

    A compound that has the general formula R3N, where R may be H or a hydrocarbon group. (Section 16.7)

  • annulenes

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

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • chemical equilibrium

    A state of dynamic balance in which the rate of formation of the products of a reaction from the reactants equals the rate of formation of the reactants from the products; at equilibrium the concentrations of the reactants and products remain constant. (Section 4.1;Chapter 15: Introduction)

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • colligative property

    A property of a solvent (vapor-pressure lowering, freezing-point lowering, boiling-point elevation, osmotic pressure) that depends on the total concentration of solute particles present. (Section 13.5)

  • Curved arrow

    A symbol used to show the redistribution of valence electrons in resonance contributing structures or reactions, symbolizing movement of two electrons

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • Eclipsed conformation

    A conformation about a carboncarbon single bond in which the atoms or groups on one carbon are as close as possible to the atoms or groups on an adjacent carbon.

  • Electrophile

    From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Lewis structure

    A representation of covalent bonding in a molecule that is drawn using Lewis symbols. Shared electron pairs are shown as lines, and unshared electron pairs are shown as pairs of dots. Only the valence-shell electrons are shown. (Section 8.3)

  • Lewis symbol (electron-dot symbol)

    The chemical symbol for an element, with a dot for each valence electron. (Section 8.1)

  • nucleotide

    Compounds formed from a molecule of phosphoric acid, a sugar molecule, and an organic nitrogen base. Nucleotides form linear polymers called DNA and RNA, which are involved in protein synthesis and cell reproduction. (Section 24.10)

  • primary alkyl halide

    An organohalide in which the alpha (a) position is connected to only one alkyl group.

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • Reductive elimination

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

  • SN1 reaction

    A unimolecular nucleophilic substitution reaction.

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