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Solutions for Chapter 6.2: nomEnClaturE of EnantiomErs

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 6.2: nomEnClaturE of EnantiomErs

Solutions for Chapter 6.2
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Since 2 problems in chapter 6.2: nomEnClaturE of EnantiomErs have been answered, more than 8152 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6.2: nomEnClaturE of EnantiomErs includes 2 full step-by-step solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781936221349. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • absorption spectrum

    A pattern of variation in the amount of light absorbed by a sample as a function of wavelength. (Section 23.5)

  • bimolecular reaction.

    An elementary step that involves two molecules. (13.5)

  • chemical reaction.

    A process in which a substance (or substances) is changed into one or more new substances. (3.7)

  • chiral.

    Compounds or ions that are not superimposable with their mirror images. (23.4)

  • combination reaction

    A chemical reaction in which two or more substances combine to form a single product. (Section 3.2)

  • critical pressure (Pc).

    The minimum pressure necessary to bring about liquefaction at the critical temperature. (11.8)

  • Cycloaddition reaction

    A reaction in which two reactants add together in a single step to form a cyclic product. The best known of these is the Diels-Alder reaction

  • disaccharide

    Carbohydrates comprisedof two monosaccharide units joined via aglycosidic linkage between the anomeric carbonof one monosaccharide and a hydroxyl group ofthe other monosaccharide.

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • Fingerprint region

    Vibrations in the region 1500 to 400 cm21 of an IR spectrum are complex and diffi cult to analyze but are characteristic for different molecules.

  • formation constant

    For a metal ion complex, the equilibrium constant for formation of the complex from the metal ion and base species present in solution. It is a measure of the tendency of the complex to form. (Section 17.5)

  • Hybrid orbital

    An orbital formed by the combination of two or more atomic orbitals.

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • interstitial alloy

    An alloy in which smaller atoms fit into spaces between larger atoms. The larger atoms are metallic elements and the smaller atoms are typically nonmetallic elements. (Section 12.3)

  • micelle

    A group of molecules arranged in a sphere such that the surface of the sphere is comprised of polar groups, rendering the micelle water soluble.

  • molecular formula

    A chemical formula that indicates the actual number of atoms of each element in one molecule of a substance. (Section 2.6)

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • VSEPR theory

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

  • ylide

    A compound with two oppositely charged atoms adjacent to each other.

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