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Solutions for Chapter 5.7SE: 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 5.7SE

Solutions for Chapter 5.7SE
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Since 2 problems in chapter 5.7SE have been answered, more than 67730 students have viewed full step-by-step solutions from this chapter. 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. Chapter 5.7SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • band theory.

    Delocalized electrons move freely through “bands” formed by overlapping molecular orbitals. (21.3)

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • bond length.

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

  • chemical property.

    Any property of a substance that cannot be studied without converting the substance into some other substance. (1.6)

  • electron affinity

    The energy change that occurs when an electron is added to a gaseous atom or ion. (Section 7.5)

  • frontier orbitals

    The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) that participate in a reaction.

  • hemiacetal

    A compound containing a hydroxyl group (OH) and an alkoxy group (OR) connected to the same carbon atom.

  • hydride ion

    An ion formed by the addition of an electron to a hydrogen atom: H-. (Section 7.7)

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • leaving group

    A group capable ofseparating from a compound.

  • methyl shift

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

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • nuclear model

    Model of the atom with a nucleus containing protons and neutrons and with electrons in the space outside the nucleus. (Section 2.2)

  • positron emission

    A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)

  • reaction rate

    A measure of the decrease in concentration of a reactant or the increase in concentration of a product with time. (Section 14.2)

  • resolution

    The separation of enantiomers from a mixture containing both enantiomers.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • Unsaturated hydrocarbon

    A hydrocarbon containing one or more carbon-carbon double or triple bonds. The three classes of unsaturated hydrocarbons are alkenes, alkynes, and arenes

Textbook Survival Guides

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