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Chemistry: An Introduction to General, Organic, and Biological Chemistry 12th Edition - Solutions by Chapter

Chemistry: An Introduction to General, Organic, and Biological Chemistry | 12th Edition | ISBN: 9780321908445 | Authors: Karen C. Timberlake

Full solutions for Chemistry: An Introduction to General, Organic, and Biological Chemistry | 12th Edition

ISBN: 9780321908445

Chemistry: An Introduction to General, Organic, and Biological Chemistry | 12th Edition | ISBN: 9780321908445 | Authors: Karen C. Timberlake

Chemistry: An Introduction to General, Organic, and Biological Chemistry | 12th Edition - Solutions by Chapter

Since problems from 18 chapters in Chemistry: An Introduction to General, Organic, and Biological Chemistry have been answered, more than 9639 students have viewed full step-by-step answer. This textbook survival guide was created for the textbook: Chemistry: An Introduction to General, Organic, and Biological Chemistry, edition: 12. The full step-by-step solution to problem in Chemistry: An Introduction to General, Organic, and Biological Chemistry were answered by , our top Chemistry solution expert on 03/09/18, 07:27PM. This expansive textbook survival guide covers the following chapters: 18. Chemistry: An Introduction to General, Organic, and Biological Chemistry was written by and is associated to the ISBN: 9780321908445.

Key Chemistry Terms and definitions covered in this textbook
  • acidic cleavage

    A reaction in which bonds are broken in the presence of an acid. For example, in the presence of a strong acid, an ether is converted into two alkyl halides.

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • branched polymer

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

  • coplanar

    Atoms that lie in the same plane.

  • dipole moment (m)

    The amount of partial charge (d ) on either end of a dipole multiplied by the distance of separation (d): m=d × d

  • E2

    A bimolecular b-elimination reaction.

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • glucose

    A polyhydroxy aldehyde whose formula is CH2OH1CHOH24CHO; it is the most important of the monosaccharides. (Section 24.8)

  • glycoside

    An acetal that is obtained by treating the cyclic hemiacetal form of a monosaccharide with an alcohol under acid-catalyzed conditions.

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • 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.

  • Molecular dipole moment (m)

    The vector sum of individual bond dipoles.

  • parent ion

    In mass spectrometry,the ion that is generated when the compound is ionized.

  • Peptide bond

    The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid

  • photon

    The smallest increment (a quantum) of radiant energy; a photon of light with frequency n has an energy equal to hn. (Section 6.2)

  • radical

    A chemical entity with an unpaired electron.

  • reduction

    A process in which a substance gains one or more electrons. (Section 4.4)

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • unsymmetrical ether

    An ether(R!O!R) where the two R groups are notidentical.

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