Solutions for Chapter 8.3: StructureS of alkyl halideS, alcoholS, thiolS, etherS, and SulfideS

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 8.3: StructureS of alkyl halideS, alcoholS, thiolS, etherS, and SulfideS

Solutions for Chapter 8.3
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781936221349. Chapter 8.3: StructureS of alkyl halideS, alcoholS, thiolS, etherS, and SulfideS includes 2 full step-by-step solutions. Since 2 problems in chapter 8.3: StructureS of alkyl halideS, alcoholS, thiolS, etherS, and SulfideS have been answered, more than 9441 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Alcohol

    A compound containing an !OH (hydroxyl) group bonded to a carbon atom

  • atom.

    The basic unit of an element that can enter into chemical combination. (2.2)

  • atomic radius

    An estimate of the size of an atom. See bonding atomic radius. (Section 7.3)

  • Bile acid

    A cholesterol-derived detergent molecule, such as cholic acid, which is secreted by the gallbladder into the intestine to assist in the absorption of dietary lipids.

  • Brønsted-Lowry base

    A proton acceptor

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • cation

    A structure that bears a positive charge.

  • chemical kinetics.

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)

  • ester

    An organic compound that has an OR group attached to a carbonyl; it is the product of a reaction between a carboxylic acid and an alcohol. (Section 24.4)

  • 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.

  • kinetic control

    A reaction for which the product distribution is determined by the relative rates at which the products are formed.

  • Kinetic control

    Experimental conditions under which the composition of the product mixture is determined by the relative rates of formation of each product.

  • kinetic energy

    The energy that an object possesses by virtue of its motion. (Section 5.1)

  • mass

    A measure of the amount of material in an object. It measures the resistance of an object to being moved. In SI units, mass is measured in kilograms. (Section 1.4)

  • molecular weight

    The mass of the collection of atoms represented by the chemical formula for a molecule. (Section 3.3)

  • Node

    A point in space where the value of a wave function is zero

  • nuclear magnetic resonance (NMR)

    A form of spectroscopy that involves the study of the interaction between electromagnetic radiation and the nuclei of atoms.

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • retro-aldol reaction

    The reverse of an aldol reaction. A b-hydroxyketone or aldehyde is converted into two ketones or aldehydes.

  • tertiary alkyl halide

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

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