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Solutions for Chapter 4.1: CisTrans Isomers Result From Restricted Rotation

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 4.1: CisTrans Isomers Result From Restricted Rotation

Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Since 8 problems in chapter 4.1: CisTrans Isomers Result From Restricted Rotation have been answered, more than 37712 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. Chapter 4.1: CisTrans Isomers Result From Restricted Rotation includes 8 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • Aldonic acid

    The product formed when the !CHO group of an aldose is oxidized to a !COOH group

  • Atropisomers

    Enantiomers that lack a chiral center and differ because of hindered rotation.

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • Conjugate addition

    Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • electron configuration

    The arrangement of electrons in the orbitals of an atom or molecule (Section 6.8)

  • entropy

    The measure of disorder associated with a system.

  • ferrimagnetism

    A form of magnetism in which unpaired electron spins on different-type ions point in opposite directions but do not fully cancel out. (Section 23.1)

  • Hydrogen bonding

    The attractive interaction between a hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of high electronegativity (again, most commonly O or N).

  • Methylene

    A !CH2! group.

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • Molecular orbital (MO) theory

    A theory of chemical bonding in which electrons in molecules occupy molecular orbitals that extend over the entire molecule and are formed by the combination of the atomic orbitals that make up the molecule

  • organic chemistry

    The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)

  • peptide bond

    The amide linkage by which two amino acids are coupled together to form peptides.

  • protein

    A biopolymer formed from amino acids. (Section 24.7)

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • Secondary structure of proteins

    The ordered arrangements (conformations) of amino acids in localized regions of a polypeptide or protein

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.

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