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Solutions for Chapter 5.3: Isomerism in Alkenes

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 5.3: Isomerism in Alkenes

Solutions for Chapter 5.3
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This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 2 problems in chapter 5.3: Isomerism in Alkenes have been answered, more than 69985 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 5.3: Isomerism in Alkenes includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • bond order

    The number of bonding electron pairs shared between two atoms, minus the number of antibonding electron pairs: bond order = (number of bonding electrons - number of antibonding electrons)/2. (Section 9.7)

  • chemical reaction.

    A process in which a substance (or substances) is changed into one or more new substances. (3.7)

  • d-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the right.

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • exo

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

  • Fischer esterifi cation

    The process of forming an ester by refl uxing a carboxylic acid and an alcohol in the presence of an acid catalyst, commonly H2SO4, ArSO3H, or HCl

  • gas

    Matter that has no fixed volume or shape; it conforms to the volume and shape of its container. (Section 1.2)

  • ion

    Electrically charged atom or group of atoms (polyatomic ion); ions can be positively or negatively charged, depending on whether electrons are lost (positive) or gained (negative) by the atoms. (Section 2.7)

  • Ligand

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

  • percent ionization

    The percent of a substance that undergoes ionization on dissolution in water. The term applies to solutions of weak acids and bases. (Section 16.6)

  • Protic acid

    An acid that is a proton donor in an acidbase reaction.

  • rate constant

    A constant of proportionality between the reaction rate and the concentrations of reactants that appear in the rate law. (Section 14.3)

  • Ring current

    An applied magnetic fi eld causes the p electrons of an aromatic ring to circulate, giving rise to the so-called ring current and an associated magnetic fi eld that opposes the applied fi eld in the middle of the ring but reinforces the applied fi eld on the outside of the ring.

  • SN1

    A unimolecular nucleophilic substitution reaction.

  • symmetric stretching

    In IR spectroscopy, when two bonds are stretching in phase with each other.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

  • triplet

    In NMR spectroscopy, a signal that is comprised of three peaks.