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Solutions for Chapter 15.1SE: 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 15.1SE

Solutions for Chapter 15.1SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 15.1SE have been answered, more than 67833 students have viewed full step-by-step solutions from this chapter. Chapter 15.1SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • adsorption

    The binding of molecules to a surface. (Section 14.7)

  • aqueous solution.

    A solution in which the solvent is water. (4.1)

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • Equatorial bond

    A bond to a chair conformation of cyclohexane that extends from the ring roughly perpendicular to the imaginary axis through the center of the ring; a bond that lies roughly along the equator of a cyclohexane ring

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • graft copolymer

    A polymer that contains sections of one homopolymer that have been grafted onto a chain of the other homopolymer.

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • intermediate

    A substance formed in one elementary step of a multistep mechanism and consumed in another; it is neither a reactant nor an ultimate product of the overall reaction. (Section 14.6)

  • Meta (m)

    Refers to groups occupying 1,3-positions on a benzene ring.

  • nuclear magnetic resonance (NMR)

    A form of spectroscopy that involves the study of the interaction between electromagnetic radiation and the nuclei of atoms.

  • oxidation–reduction (redox) reaction

    A chemical reaction in which the oxidation states of certain atoms change. (Section 4.4; Chapter 20: Introduction)

  • peptide bond

    The amide linkage by which two amino acids are coupled together to form peptides.

  • polycarbonates

    Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons

  • Polyunsaturated triglyceride

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

  • potential energy

    The energy that an object possesses as a result of its composition or its position with respect to another object. (Section 5.1)

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • scientific method

    The general process of advancing scientific knowledge by making experimental observations and by formulating hypotheses, theories, and laws. (Section 1.3)

  • secondary alkyl halide

    An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.

  • symmetric stretching

    In IR spectroscopy, when two bonds are stretching in phase with each other.

  • Vinylic carbocation

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

Textbook Survival Guides

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