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Solutions for Chapter Chapter 17: Reactions of Aromatic Compounds

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321811394

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Solutions for Chapter Chapter 17: Reactions of Aromatic Compounds

Solutions for Chapter Chapter 17
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Textbook: Organic Chemistry
Edition: 8
Author: L.g. Wade, Jr.
ISBN: 9780321811394

This expansive textbook survival guide covers the following chapters and their solutions. Chapter Chapter 17: Reactions of Aromatic Compounds includes 71 full step-by-step solutions. Since 71 problems in chapter Chapter 17: Reactions of Aromatic Compounds have been answered, more than 22608 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Organic Chemistry was written by and is associated to the ISBN: 9780321811394.

Key Chemistry Terms and definitions covered in this textbook
  • Aldose

    A monosaccharide containing an aldehyde group

  • Avogadro’s number (NA).

    6.022 3 1023; the number of particles in a mole. (3.2)

  • bonding molecular orbital.

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

  • conjugate acid

    In an acid-base reaction, the product that results when a base is protonated.

  • core electrons

    The electrons that are not in the outermost shell of an atom. (Section 6.8)

  • Curved arrow

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

  • debye (D)

    A unit of measure fordipole moments, where 1 debye = 10-18 esu×cm.

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • downfield

    The left side of an NMR spectrum.

  • fats

    Triglycerides that are solids atroom temperature.

  • hemiacetal

    A compound containing a hydroxyl group (OH) and an alkoxy group (OR) connected to the same carbon atom.

  • internal alkyne

    A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.

  • Messenger RNA (mRNA)

    A ribonucleic acid that carries coded genetic information from DNA to the ribosomes for the synthesis of proteins

  • nitration

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

  • overlap

    The extent to which atomic orbitals on different atoms share the same region of space. When the overlap between two orbitals is large, a strong bond may be formed. (Section 9.4)

  • photon

    When electromagnetic radiation is viewed as a particle, an individual packet of energy.

  • Protic solvent

    A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.

  • rearrangement

    One of the four arrow-pushing patterns for ionic reactions.

  • Shielding in NMR

    Also called diamagnetic shielding; the term refers to the reduction in magnetic fi eld strength experienced by a nucleus underneath electron density induced to circulate when the molecule is placed in a strong magnetic fi eld.

  • strong deactivators

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

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