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Solutions for Chapter 24.4SE: 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 24.4SE

Solutions for Chapter 24.4SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 24.4SE have been answered, more than 67796 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 24.4SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amino acid

    A carboxylic acid that contains an amino 1¬NH22 group attached to the carbon atom adjacent to the carboxylic acid 1¬COOH2 functional group. (Section 24.7)

  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • Aufbau principle

    A rule that determines the order in which orbitals are filled by electrons. Specifically, the lowest energy orbital is filled first.

  • b-Elimination

    A reaction in which a molecule, such as HCl, HBr, HI, or HOH, is split out or eliminated from adjacent carbons

  • Benzylic position

    An sp3 -hybridized carbon bonded to a benzene ring

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • Haloalkane (alkyl halide)

    A compound containing a halogen atom covalently bonded to an sp3 -hybridized carbon atom. Given the symbol R!X.

  • hydride ion

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

  • nucleophilic aromatic substitution

    A substitution reaction in which an aromatic ring is attacked by a nucleophile, which replaces a leaving group.

  • Nucleoside

    A building block of nucleic acids, consisting of d-ribose or 2-deoxy-d-ribose bonded to a heterocyclic aromatic amine base by a b-N-glycosidic bond

  • nucleosides

    The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).

  • optically inactive

    A compound that does not rotate plane-polarized light.

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • polyprotic acid

    A substance capable of dissociating more than one proton in water; H2SO4 is an example. (Section 16.6)

  • reaction quotient (Q)

    The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)

  • resonance

    A method that chemists use to deal with the inadequacy of bond-line drawings.

  • sigmatropic rearrangements

    A pericyclic reaction in which one s bond is formed at the expense of another.

  • syn addition

    An addition reaction in which two groups are added to the same face of a p bond.

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

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