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Solutions for Chapter 7.4: The Reactivity of Alkynes

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 7.4: The Reactivity of Alkynes

Solutions for Chapter 7.4
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Organic Chemistry was written by and is associated to the ISBN: 9780134042282. Chapter 7.4: The Reactivity of Alkynes includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Since 2 problems in chapter 7.4: The Reactivity of Alkynes have been answered, more than 31217 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • aldose

    A carbohydrate that contains an aldehyde group.

  • alpha particles

    Particles that are identical to helium-4 nuclei, consisting of two protons and two neutrons, symbol 4 2He or 4 2a. (Section 21.1)

  • anomeric carbon

    The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • chlorofluorocarbons

    Compounds composed entirely of chlorine, fluorine, and carbon. (Section 18.3)

  • compound.

    A substance composed of atoms of two or more elements chemically united in fixed proportions. (1.4)

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • Double helix

    A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis

  • Edman degradation

    A method for analyzing the sequence of amino acids in apeptide by removing one amino acid residue at a time and identifying each residue as it is removed.

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • Gilman reagent

    A lithium dialkyl cuprate (R2CuLi).

  • 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.

  • Hemiacetal

    A molecule containing an !OH and an !OR or !OAr group bonded to the same carbon

  • Hydration

    The addition of water.

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • mass number

    The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)

  • nitrogen rule

    In mass spectrometry, an odd molecular weight indicates an odd number of nitrogen atoms in the compound, while an even molecular weight indicates either an even number of nitrogen atoms or the absence of nitrogen.

  • physiological pH

    The pH of blood (approximately 7.3).

  • saponification

    Hydrolysis of an ester in the presence of a base. (Section 24.4)

  • solution

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

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