×
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 1.3: Structures of Covalent Compounds

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 1.3: Structures of Covalent Compounds

Chapter 1.3: Structures of Covalent Compounds includes 4 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Since 4 problems in chapter 1.3: Structures of Covalent Compounds have been answered, more than 31626 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Aldehyde

    A compound containing a !CHO group

  • alpha (a) rays.

    Helium ions with a positive charge of 12. (2.2)

  • anode.

    The electrode at which oxidation occurs. (18.2)

  • antibonding molecular orbital.

    A molecular orbital that is of higher energy and lower stability than the atomic orbitals from which it was formed. (10.6)

  • Chiral

    From the Greek, cheir meaning hand; an object that is not superposable on its mirror image; an object that has handedness.

  • delocalized molecular orbitals.

    Molecular orbitals that are not confined between two adjacent bonding atoms but actually extend over three or more atoms. (10.8)

  • DEPT 13C NMR

    In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • Gauche conformation

    A conformation about a single bond of an alkane in which two groups on adjacent carbons lie at a dihedral angle of 60°

  • hydrochlorofluorocarbons, (HCFCs)

    Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.

  • induction

    The withdrawal of electron density that occurs when a bond is shared by two atoms of differing electronegativity.

  • momentum

    The product of the mass, m, and velocity, v, of an object. (Section 6.4)

  • nitration

    An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.

  • norbornane

    The common name for bicyclo[2.2.1]heptane.

  • Polysaccharide

    A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.

  • rate-determining step

    The slowest elementary step in a reaction mechanism. (Section 14.6)

  • resonance hybrid

    A term used to describe the character of a chemical entity (molecule, ion, or radical) exhibiting more than one significant resonance structure.

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • saturated

    A compound that contains no p bonds.

  • strong deactivators

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

×
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