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Solutions for Chapter 18.7: Acidity of phenols

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 18.7: Acidity of phenols

Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 18.7: Acidity of phenols includes 3 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Since 3 problems in chapter 18.7: Acidity of phenols have been answered, more than 33945 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • absorption spectrum

    In IR spectroscopy as well as UV-VIS spectroscopy, a plot that measures the percent transmittance or absorption as a function of frequency.

  • acetoacetic ester synthesis

    A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.

  • active site

    Specific site on a heterogeneous catalyst or an enzyme where catalysis occurs. (Section 14.7)

  • amide

    An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)

  • Angle strain

    The strain that arises when a bond angle is either compressed or expanded compared to its optimal value.

  • anion

    A negatively charged ion. (Section 2.7)

  • atom.

    The basic unit of an element that can enter into chemical combination. (2.2)

  • base peak

    In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.

  • beta (b) position

    The position immediately adjacent to an alpha (a) position.

  • block copolymer

    A copolymer in which the different homopolymer subunits are connected together in one chain.

  • chemical kinetics

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (Chapter 14: Introduction)

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • Crystalline domain

    An ordered crystalline region in the solid state of a polymer. Also called a crystallite.

  • Curved arrow

    A symbol used to show the redistribution of valence electrons in resonance contributing structures or reactions, symbolizing movement of two electrons

  • Dehydrohalogenation

    Removal of !H and !X from adjacent carbons; a type of b-elimination

  • free induction decay

    In NMR spectroscopy, a complex signal which is a combination of all of the electrical impulses generated by each type of proton.

  • 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

  • Optical purity

    The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.

  • sigmatropic rearrangements

    A pericyclic reaction in which one s bond is formed at the expense of another.

  • superimposable

    Two objects that are identical.

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