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Solutions for Chapter 7.1: The Nomenclature of Alkynes

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 7.1: The Nomenclature of Alkynes

Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 9 problems in chapter 7.1: The Nomenclature of Alkynes have been answered, more than 42430 students have viewed full step-by-step solutions from this chapter. Chapter 7.1: The Nomenclature of Alkynes includes 9 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: 7.

Key Chemistry Terms and definitions covered in this textbook
  • Acyl group

    An RCO! or ArCO! group.

  • beta elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • bomb calorimeter

    A device for measuring the heat evolved in the combustion of a substance under constant-volume conditions. (Section 5.5)

  • cathode rays

    Streams of electrons that are produced when a high voltage is applied to electrodes in an evacuated tube. (Section 2.2)

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • geometric isomerism

    A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)

  • lattice vectors

    The vectors a, b, and c that define a crystal lattice. The position of any lattice point in a crystal can be represented by summing integer multiples of the lattice vectors. (Section 12.2)

  • levorotatory, or merely levo or l

    A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the left (counterclockwise). (Section 24.4)

  • peptide

    A chain comprised of a small number of amino acid residues.

  • photodissociation

    The breaking of a molecule into two or more neutral fragments as a result of absorption of light. (Section 18.2)

  • polyurethanes

    Polymers made up of repeating urethane groups, also sometimes called carbamate groups (!N!CO2!).

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

  • Reaction coordinate diagram

    A graph showing the energy changes that occur during a chemical reaction; energy is plotted on the vertical axis and reaction progress is plotted on the horizontal axis.

  • Schiff base

    An alternative name for an imine

  • Steric strain

    The strain that arises when nonbonded atoms separated by four or more bonds are forced closer to each other than their atomic (contact) radii would allow. Steric strain is also called non-bonded interaction strain, or van der Waals strain.

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • Vinyl group

    A carbocation in which the positive charge is on one of the carbons of a carbon-carbon double bond.

  • vinylic

    The carbon atoms of a carbon-carbon double bond.

  • VSEPR theory

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

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.