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Solutions for Chapter 5.11SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 5.11SE

Solutions for Chapter 5.11SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 5.11SE have been answered, more than 65296 students have viewed full step-by-step solutions from this chapter. Chapter 5.11SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activity series.

    A summary of the results of many possible displacement reactions. (4.4)

  • Aglycon

    Lacking a sugar

  • alkylthio group

    An SR group.

  • estrogens

    Female sex hormones.

  • exergonic

    Any process with a negative DG.

  • fishhook arrow

    A curved arrow with only one barb, indicating the motion of just one electron (also see Sect. 11.1).

  • Friedel-Crafts reaction

    An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.

  • halogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.

  • Ka

    A measure of the strength of an acid: Ka = Keq 3H2O4 = 3H3O+ 4 3A- 4 3HA4

  • lone pair

    A pair of unshared, or nonbonding, electrons.

  • Michael reaction

    A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.

  • microstate

    The state of a system at a particular instant; one of many possible energetically equivalent ways to arrange the components of a system to achieve a particular state. (Section 19.3)

  • oxidizing agent, or oxidant

    The substance that is reduced and thereby causes the oxidation of some other substance in an oxidation–reduction reaction. (Section 20.1)

  • 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

  • pH

    The negative log in base 10 of the aquated hydrogen ion concentration: pH = -log3H+4. (Section 16.4)

  • phospholipid

    A form of lipid molecule that contains charged phosphate groups. (Section 24.9)

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • spin-spin splitting

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms, in which the multiplicity of each signal is affected by the other.

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule

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