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Solutions for Chapter 25.1: THIOESTERS

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 25.1: THIOESTERS

Solutions for Chapter 25.1
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Chapter 25.1: THIOESTERS includes 2 full step-by-step solutions. Since 2 problems in chapter 25.1: THIOESTERS have been answered, more than 34355 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: 6. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • alkanes.

    Hydrocarbons having the general formula CnH2n12, where n 5 1,2, . . . . (24.2)

  • Allylic substitution

    Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.

  • Brønsted–Lowry acid

    A substance (molecule or ion) that acts as a proton donor. (Section 16.2)

  • Chain length

    The number of times the cycle of chain propagation steps repeats in a chain reaction.

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • Circular DNA

    A type of double-stranded DNA in which the 59 and 39 ends of each strand are joined by phosphodiester groups.

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • exo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.

  • 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)

  • Hydration

    The addition of water.

  • Lactone

    A cyclic ester.

  • lone pair

    A pair of unshared, or nonbonding, electrons.

  • Monomer

    From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.

  • radial probability function

    The probability that the electron will be found at a certain distance from the nucleus. (Section 6.6)

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • reaction mechanism

    A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • S

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A counterclockwise sequence for 1-2-3 is designated as S.

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

  • Tesla (T)

    The SI unit for magnetic fi eld strength.

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