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Solutions for Chapter 13.20: Introduction to Infrared Spectroscopy

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 13.20: Introduction to Infrared Spectroscopy

Solutions for Chapter 13.20
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Since 1 problems in chapter 13.20: Introduction to Infrared Spectroscopy have been answered, more than 33996 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: 9. Chapter 13.20: Introduction to Infrared Spectroscopy includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • Absolute confi guration

    Which of the two possible isomers an enantiomer is (i.e., whether it is the right- or left-handed isomer).

  • accuracy

    A measure of how closely individual measurements agree with the correct value. (Section 1.5)

  • bimolecular reaction.

    An elementary step that involves two molecules. (13.5)

  • Boyle’s law.

    The volume of a fixed amount of gas maintained at constant temperature is inversely proportional to the gas pressure. (5.3)

  • chelate effect

    The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)

  • Conjugate base

    The species formed when an acid transfers a proton to a base

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • electromotive force (emf)

    A measure of the driving force, or electrical pressure, for the completion of an electrochemical reaction. Electromotive force is measured in volts: 1 V = 1 J>C. Also called the cell potential. (Section 20.4)

  • Friedel-Crafts alkylation

    An electrophilic aromatic substitution reaction that installs an alkyl group on an aromatic ring.

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • matter waves

    The term used to describe the wave characteristics of a moving particle. (Section 6.4)

  • melt transition temperature (Tm)

    The temperature at which the crystallineregions of a polymer become amorphous.

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • Organometallic compound

    A compound that contains a carbon-metal bond.

  • Polynuclear aromatic hydrocarbon (PAH)

    A hydrocarbon containing two or more fused benzene rings

  • Polyurethane

    A polymer containing the !NHCO2! group as a repeating unit

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

  • radical inhibitor

    A compound that prevents a radical chain process from either getting started or continuing.

  • solvent

    The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)

  • unsymmetrical ether

    An ether(R!O!R) where the two R groups are notidentical.

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