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Solutions for Chapter 11: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 11

Solutions for Chapter 11
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Textbook: Chemistry: The Central Science
Edition: 13
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus
ISBN: 9780321910417

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Since 219 problems in chapter 11 have been answered, more than 310122 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 11 includes 219 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkyl halide

    An organic compound containing at least one halogen.

  • chemical energy.

    Energy stored within the structural units of chemical substances. (6.1)

  • Chemical shift (d)

    The shift in parts per million of an NMR signal relative to the signal of TMS

  • Conjugate addition

    Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • crystalline solid (crystal)

    A solid whose internal arrangement of atoms, molecules, or ions possesses a regularly repeating pattern in any direction through the solid. (Section 12.2)

  • double bond

    A covalent bond involving two electron pairs. (Section 8.3)

  • E2

    A bimolecular eliminationreaction.eclipsed conformation (Sect. 4.7): A conformationin which groups are eclipsing each other in aNewman projection.

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • Halohydrin

    A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.

  • Le Châtelier’s principle

    A principle stating that when we disturb a system at chemical equilibrium, the relative concentrations of reactants and

  • lone pair

    A pair of unshared, or nonbonding, electrons.

  • Nucleotide

    A nucleoside in which a molecule of phosphoric acid is esterifi ed with an !OH of the monosaccharide, most commonly either the 39!OH or the 59!OH.

  • rate equation

    An equation thatdescribes the relationship between the rate of a reactionand the concentration of reactants.

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • Reductive amination

    A method for preparing substituted amines by treating an aldehyde or ketone with an amine in the presence of a reducing agent

  • s-cis

    A conformation of a conjugated diene in which the disposition of the two p bonds with regard to the connecting single bond is cis-like (a dihedral angle of 0°).

  • sp2 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and two 2p atomic orbitals.

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule