Solutions for Chapter 6.1SE: 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 6.1SE

Solutions for Chapter 6.1SE
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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 Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 6.1SE have been answered, more than 108667 students have viewed full step-by-step solutions from this chapter. Chapter 6.1SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amorphous

    A region of a polymer in which nearby chains are not linearly extended and are not parallel to one another.

  • aryl amine

    An amine in which the nitrogen atom is connected directly to an aromatic ring.

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • bond length.

    The distance between the nuclei of two bonded atoms in a molecule. (9.4)

  • Carbanion

    An ion in which carbon has an unshared pair of electrons and bears a negative charge.

  • deshielded

    In NMR spectroscopy,protons or carbon atoms whose surrounding electron density is poor.

  • 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

  • electrostatic potential maps

    A three-dimensional, rainbowlike image used to visualize partial charges in a compound.

  • elemental semiconductor

    A semiconducting material composed of just one element. (Section 12.7)

  • enthalpy

    A quantity defined by the relationship H = E + PV; the enthalpy change, ?H, for a reaction that occurs at constant pressure is the heat evolved or absorbed in the reaction: ?H = qp. (Section 5.3)

  • f-block metals

    Lanthanide and actinide elements in which the 4f or 5f orbitals are partially occupied. (Section 6.9)

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • hydrochlorofluorocarbons, (HCFCs)

    Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.

  • linkage isomers

    Structural isomers of coordination compounds in which a ligand differs in its mode of attachment to a metal ion. (Section 23.4)

  • Lipid bilayer

    A back-to-back arrangement of phospholipid monolayers, often forming a closed vesicle or membrane.

  • metathesis (exchange) reaction

    A reaction in which two substances react through an exchange of their component ions: AX + BY ¡ AY + BX. Precipitation and acid–base neutralization reactions are examples of metathesis reactions. (Section 4.2)

  • methyl shift

    A type of carbocation rearrangement in which a methyl group migrates.

  • secondary

    A term used to indicate that exactly two alkyl groups are attached directly to a particular position. For example, a secondary carbocation has two alkyl groups attached directly to the electrophilic carbon atom (C+).

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • Wavenumbers (—n )

    The frequency of electromagnetic radiation expressed as the number of waves per centimeter, with units cm21 (read: reciprocal centimeters).

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