×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 5.4: Naming Alkenes Using the E,Z System

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 5.4: Naming Alkenes Using the E,Z System

Chapter 5.4: Naming Alkenes Using the E,Z System includes 7 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 7 problems in chapter 5.4: Naming Alkenes Using the E,Z System have been answered, more than 38139 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: 7.

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

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

  • Allene

    The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.

  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • atactic

    A polymer in which the repeating units contain chirality centers which are not arranged in a pattern (they have random configurations).

  • Conjugated

    A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • 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.

  • gas chromatograph – mass spectrometer

    A device used for the analysis of a mixture that contains several compounds.

  • Lindlar catalyst

    Finely powdered palladium metal deposited on solid calcium carbonate that has been specially modifi ed with lead salts. Its particular use is as a catalyst for the reduction of an alkyne to a cis alkene

  • molar mass

    The mass of one mole of a substance in grams; it is numerically equal to the formula weight in atomic mass units. (Section 3.4)

  • N-nitrosamine

    A compound with the structure R2N!NRO.

  • neutron

    An electrically neutral particle found in the nucleus of an atom; it has approximately the same mass as a proton. (Section 2.3)

  • nucleosides

    The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).

  • rate constant

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

  • Reduction

    The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • superimposable

    Two objects that are identical.

  • symmetry allowed

    A reaction that obeys conservation of orbital symmetry.

  • thiols

    Compounds containing a mercapto group (SH).

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password