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Solutions for Chapter 10.4SE: 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 10.4SE

Solutions for Chapter 10.4SE
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Chapter 10.4SE includes 2 full step-by-step solutions. Since 2 problems in chapter 10.4SE have been answered, more than 65257 students have viewed full step-by-step solutions from this chapter. 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.

Key Chemistry Terms and definitions covered in this textbook
  • Aprotic solvent

    A solvent that cannot serve as a hydrogen-bond donor; nowhere in the molecule is there a hydrogen bonded to an atom of high electronegativity. Common aprotic solvents are dichloromethane, diethyl ether, and dimethyl sulfoxide

  • Celsius scale

    A temperature scale on which water freezes at 0° and boils at 100° at sea level. (Section 1.4)

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • complex ion.

    An ion containing a central metal cation bonded to one or more molecules or ions. (16.10)

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • enamine

    A compound containing a nitrogen atom directly connected to a carboncarbon p bond.

  • enantiomers

    Two mirror-image molecules of a chiral substance. The enantiomers are nonsuperimposable. (Section 23.4)

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • Hund’s rule

    A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)

  • Living polymer

    A polymer chain that continues to grow without chain-termination steps until either all of the monomer is consumed or some external agent is added to terminate the chain. The polymer chains will continue to grow if more monomer is added.

  • Low-density lipoprotein (LDL)

    Plasma particles, density 1.02–1.06 g/mL, consisting of approximately 26% proteins, 50% cholesterol, 21% phospholipids, and 4% triglycerides.

  • mixture

    A combination of two or more substances in which each substance retains its own chemical identity. (Section 1.2)

  • N-Terminal amino acid

    The amino acid at the end of a polypeptide chain having the free !NH2 group

  • Phenol

    A compound that contains an !OH bonded to a benzene ring; a benzenol.

  • propagation

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

  • Radical cation

    A species formed when a neutral molecule loses one electron; it contains both an odd number of electrons and a positive charge.

  • 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.

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

  • thiolate

    The conjugate base of a thiol.

Textbook Survival Guides

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