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Solutions for Chapter 5.14: Dehydrohalogenation of Alkyl Halides

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 5.14: Dehydrohalogenation of Alkyl Halides

Solutions for Chapter 5.14
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Since 2 problems in chapter 5.14: Dehydrohalogenation of Alkyl Halides have been answered, more than 25437 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 5.14: Dehydrohalogenation of Alkyl Halides includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • aldose

    A carbohydrate that contains an aldehyde group.

  • 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)

  • colloids (colloidal dispersions)

    Mixtures containing particles larger than normal solutes but small enough to remain suspended in the dispersing medium. (Section 13.6)

  • 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)

  • cycloaddition reactions

    Reactions in which two p systems are joined together in a way that forms a ring. In the process, two p bonds are converted into two s bonds.

  • dipole-dipole interactions

    Theresulting net attraction between two dipoles.

  • fibrous proteins

    Proteins that consist of linear chains that are bundled together.

  • frequency

    The number of times per second that one complete wavelength passes a given point. (Section 6.1)

  • Ligand

    A Lewis base bonded to a metal atom in a coordination compound. It may bond strongly or weakly.

  • 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)

  • Michael reaction

    A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.

  • oxyacid

    A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)

  • peptide bond

    The amide linkage by which two amino acids are coupled together to form peptides.

  • periodic table

    The arrangement of elements in order of increasing atomic number, with elements having similar properties placed in vertical columns. (Section 2.5)

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • strong activators

    Groups that strongly activate an aromatic ring toward electrophilic aromatic substitution, thereby significantly enhancing the rate of the reaction.

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

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