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Solutions for Chapter Lesson 13: Isotopes

Full solutions for Living by Chemistry | 2nd Edition

ISBN: 9781464142314

Solutions for Chapter Lesson 13: Isotopes

Since 9 problems in chapter Lesson 13: Isotopes have been answered, more than 20661 students have viewed full step-by-step solutions from this chapter. Living by Chemistry was written by and is associated to the ISBN: 9781464142314. Chapter Lesson 13: Isotopes includes 9 full step-by-step solutions. This textbook survival guide was created for the textbook: Living by Chemistry, edition: 2. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • adrenocortical hormones

    Hormones that are secreted by the cortex (the outer layer) of the adrenal glands. Adrenocortical hormones are typically characterized by a carbonyl group or hydroxyl group at C11 of the steroid skeleton.

  • aryl amine

    An amine in which the nitrogen atom is connected directly to an aromatic ring.

  • Constitutional isomers

    Compounds with the same molecular formula but a different connectivity of their atoms

  • crystallite

    A region of a polymer inwhich the chains are linearly extended and closein proximity to one another, resulting in van der Waals forces that hold the chains close together.

  • Enthalpy change, DH

    The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • frontier orbitals

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

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Hofmann elimination

    A reaction in which an amino group is treated with excess methyl iodide, thereby converting it into an excellent leaving group, followed by treatment with a strong base to give an E2 reaction that yields an alkene.

  • ionic solids

    Solids that are composed of ions. (Section 12.1)

  • Keto-enol tautomerism

    A type of isomerism involving keto (from ketone) and enol tautomers

  • Meisenheimer complex

    Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.

  • monomers

    Molecules with low molecular weights, which can be joined together (polymerized) to form a polymer. (Section 12.8)

  • optically inactive

    A compound that does not rotate plane-polarized light.

  • particle accelerator

    A device that uses strong magnetic and electrostatic fields to accelerate charged particles. (Section 21.3)

  • phosphoglycerides

    Compounds that are very similar in structure to triglycerides, with the main difference being that one of the three fatty acid residues is replaced by a phosphoester group.

  • S

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A counterclockwise sequence for 1-2-3 is designated as S.

  • tertiary alkyl halide

    An organohalide in which the alpha (a) position is connected to three alkyl groups.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • VSEPR theory

    Valence Shell Electron Pair Repulsion theory, which can be used to predict the geometry around an atom.

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