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Textbooks / Chemistry / Organic Chemistry 8

Organic Chemistry 8th Edition - Solutions by Chapter

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Organic Chemistry | 8th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 331 Reviews
Textbook: Organic Chemistry
Edition: 8
Author: Paula Yurkanis Bruice
ISBN: 9780134042282

This expansive textbook survival guide covers the following chapters: 127. The full step-by-step solution to problem in Organic Chemistry were answered by , our top Chemistry solution expert on 03/16/18, 04:59PM. Organic Chemistry was written by and is associated to the ISBN: 9780134042282. Since problems from 127 chapters in Organic Chemistry have been answered, more than 21370 students have viewed full step-by-step answer. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8.

Key Chemistry Terms and definitions covered in this textbook
  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • activity series.

    A summary of the results of many possible displacement reactions. (4.4)

  • Allyl

    A !CH2CH"CH2 group.

  • Amino group

    A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms

  • chemical bond

    A strong attractive force that exists between atoms in a molecule. (Section 8.1)

  • curved arrows

    Tools that are used for drawing resonance structures and for showing the flow of electron density during each step of a reaction mechanism.

  • d-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the right.

  • dimensional analysis

    A method of problem solving in which units are carried through all calculations. Dimensional analysis ensures that the final answer of a calculation has the desired units. (Section 1.6)

  • 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 reaction

    An electrophilic aromatic substitution in which a hydrogen of an aromatic ring is replaced by an alkyl or acyl group.

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • Henderson-Hasselbalch equation

    An equation that is often employed to calculate the pH of buffered solutions: pH = pKa + log 3conjugated base4 3acid4

  • Ligand

    A Lewis base bonded to a metal atom in a coordination compound. It may bond strongly or weakly.

  • osmotic pressure

    The pressure that must be applied to a solution to stop osmosis from pure solvent into the solution. (Section 13.5)

  • plastic

    A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • regioselective

    A reaction that can produce two or more constitutional isomers but nevertheless produces one as the major product.

  • sigma 1S2 molecular orbital

    A molecular orbital that centers the electron density about an imaginary line passing through two nuclei. (Section 9.7)

  • Substitution

    A reaction in which an atom or group of atoms in a compound is replaced by another atom or group of atoms.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

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