Solutions for Chapter 17.9SE: 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 17.9SE

Solutions for Chapter 17.9SE
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 17.9SE have been answered, more than 146716 students have viewed full step-by-step solutions from this chapter. Chapter 17.9SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amphoteric

    Compounds that will react with either acids or bases. Amino acids are amphoteric.

  • antiferromagnetism

    A form of magnetism in which unpaired electron spins on adjacent sites point in opposite directions and cancel each other’s effects. (Section 23.1)

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • Brønsted-Lowry base

    A proton acceptor

  • Deshielding

    The term used to express the concept of less shielding in NMR

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • displacement reaction

    A reaction in which an element reacts with a compound, displacing an element from it. (Section 4.4)

  • electron shell

    A collection of orbitals that have the same value of n. For example, the orbitals with n = 3 (the 3s, 3p, and 3d orbitals) comprise the third shell. (Section 6.5)

  • endothermic process

    A process in which a system absorbs heat from its surroundings. (Section 5.2)

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • matter waves

    The term used to describe the wave characteristics of a moving particle. (Section 6.4)

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • Oil

    When used in the context of fats and oils, a mixture of triglycerides that is liquid at room temperature

  • oxidation–reduction (redox) reaction

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

  • polarizability

    The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)

  • Primary (1°) amine

    An amine in which nitrogen is bonded to one carbon and two hydrogens

  • systematic name

    A name that is assigned using the rules of IUPAC nomenclature.

  • Wave function

    A solution to a set of equations that defi nes the energy of an electron in an atom and the region of space it may occupy.

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