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Solutions for Chapter 3.11: Some Cycloalkanes Have Angle Strain

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 3.11: Some Cycloalkanes Have Angle Strain

Chapter 3.11: Some Cycloalkanes Have Angle Strain includes 3 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Since 3 problems in chapter 3.11: Some Cycloalkanes Have Angle Strain have been answered, more than 22563 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780321803221.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • 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)

  • basic anhydride (basic oxide)

    An oxide that forms a base when added to water; soluble metal oxides are basic anhydrides. (Section 22.5)

  • battery

    A self-contained electrochemical power source that contains one or more voltaic cells. (Section 20.7)

  • beta emission

    A nuclear decay process where a beta particle is emitted from the nucleus; also called beta decay. (Section 21.1)

  • binary compounds.

    Compounds formed from just two elements. (2.7)

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • chemical shift (d)

    In an NMR spectrum, the location of a signal, defined relative to the frequency of absorption of a reference compound, tetramethylsilane (TMS).

  • critical temperature

    The highest temperature at which it is possible to convert the gaseous form of a substance to a liquid. The critical temperature increases with an increase in the magnitude of intermolecular forces. (Section 11.4)

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • rad

    A measure of the energy absorbed from radiation by tissue or other biological material; 1 rad = transfer of 1 * 10-2 J of energy per kilogram of material. (Section 21.9)

  • radial probability function

    The probability that the electron will be found at a certain distance from the nucleus. (Section 6.6)

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • saturated solution

    A solution in which undissolved solute and dissolved solute are in equilibrium. (Section 13.2)

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

  • solution

    A mixture of substances that has a uniform composition; a homogeneous mixture. (Section 1.2)

  • substrate

    The starting alkyl halide in a substitution or elimination reaction.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

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