Solutions for Chapter 1.5SE: 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 1.5SE

Solutions for Chapter 1.5SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 1.5SE have been answered, more than 101036 students have viewed full step-by-step solutions from this chapter. 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. Chapter 1.5SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkanamine

    A format for naming primary amines containing a complex alkyl group.

  • Allylic

    Next to a carbon-carbon double bond.

  • alpha (a) position

    The position immediately adjacent to a functional group.

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • bond cleavage

    The breaking of a bond, either homolytically or heterolytically. bond dissociation energy (Sect. 6.1): The energy required to achieve homolytic bond cleavage (generating radicals).

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • critical pressure (Pc).

    The minimum pressure necessary to bring about liquefaction at the critical temperature. (11.8)

  • doublet

    In NMR spectroscopy, a signal that is comprised of two peaks.

  • enthalpy of formation

    The enthalpy change that accompanies the formation of a substance from the most stable forms of its component elements. (Section 5.7)

  • high-spin complex

    A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • ionization energy

    The energy required to remove an electron from a gaseous atom when the atom is in its ground state. (Section 7.4)

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • nuclear disintegration series

    A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one; also called a radioactive series. (Section 21.2)

  • oxyacid

    A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)

  • Polar covalent bond

    A covalent bond between atoms whose difference in electronegativity is between approximately 0.5 and 1.9.

  • primary

    A term used to indicate that exactly one alkyl group is attached directly to a particular position. For example, a primary carbocation has one alkyl group (not more) attached directly to the electrophilic carbon atom (C+).

  • propagation

    For radical reactions,the steps whose sum gives the net chemical reaction.

  • Raoult’s law

    A law stating that the partial pressure of a solvent over a solution, Psolution, is given by the vapor pressure of the pure solvent, P° solvent, times the mole fraction of a solvent in the solution, Xsolvent: Psolution = XsolventP° solvent. (Section 13.5)

  • soluble

    A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.

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