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Organic Chemistry, - Standalone Book 2nd Edition - Solutions by Chapter

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Organic Chemistry, - Standalone Book | 2nd Edition - Solutions by Chapter

This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Organic Chemistry, - Standalone Book was written by Patricia and is associated to the ISBN: 9781118452288. Since problems from 27 chapters in Organic Chemistry, - Standalone Book have been answered, more than 24734 students have viewed full step-by-step answer. The full step-by-step solution to problem in Organic Chemistry, - Standalone Book were answered by Patricia, our top Chemistry solution expert on 01/19/18, 05:12PM. This expansive textbook survival guide covers the following chapters: 27.

Key Chemistry Terms and definitions covered in this textbook
  • (PAHs)

    Compounds containing multiple aromatic rings fused together.

  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • allylic

    The positions that are adjacent to the vinylic positions of a carboncarbon double bond.

  • anion

    A negatively charged ion. (Section 2.7)

  • atomic radius

    An estimate of the size of an atom. See bonding atomic radius. (Section 7.3)

  • bond order

    The number of bonding electron pairs shared between two atoms, minus the number of antibonding electron pairs: bond order = (number of bonding electrons - number of antibonding electrons)/2. (Section 9.7)

  • branched polymer

    A polymer that contains a large number of branches connected to the main chain of the polymer.

  • buffer capacity

    The amount of acid or base a buffer can neutralize before the pH begins to change appreciably. (Section 17.2)

  • Carboxylic acid

    A compound containing a carboxyl, !COOH, group.

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • curie

    A measure of radioactivity: 1 curie = 3.7 * 1010 nuclear disintegrations per second. (Section 21.4)

  • Cycloaddition reaction

    A reaction in which two reactants add together in a single step to form a cyclic product. The best known of these is the Diels-Alder reaction

  • delocalized electrons

    Electrons that are spread over a number of atoms in a molecule or a crystal rather than localized on a single atom or a pair of atoms. (Section 9.6)

  • disaccharide

    Carbohydrates comprisedof two monosaccharide units joined via aglycosidic linkage between the anomeric carbonof one monosaccharide and a hydroxyl group ofthe other monosaccharide.

  • hole

    A vacancy in the valence band of a semiconductor, created by doping. (Section 12.7)

  • Hund’s rule

    A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)

  • ignal splitting in NMR

    Spin-spin coupling with adjacent nuclei split NMR signals depending on the extent of coupling and the number of adjacent equivalent nuclei.

  • lock-and-key model

    A model of enzyme action in which the substrate molecule is pictured as fitting rather specifically into the active site on the enzyme. It is assumed that in being bound to the active site, the substrate is somehow activated for reaction. (Section 14.7)

  • Ortho

    Refers to groups occupying l,2-positions on a benzene ring.

  • solvation

    The clustering of solvent molecules around a solute particle. (Section 13.1)

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