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Textbooks / Chemistry / Organic Chemistry 7

Organic Chemistry 7th Edition - Solutions by Chapter

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781269406772

Organic Chemistry | 7th Edition | ISBN: 9781269406772 | Authors: Paula Yurkanis Bruice

Organic Chemistry | 7th Edition - Solutions by Chapter

Organic Chemistry was written by and is associated to the ISBN: 9781269406772. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. The full step-by-step solution to problem in Organic Chemistry were answered by , our top Chemistry solution expert on 09/04/17, 10:07PM. This expansive textbook survival guide covers the following chapters: 30. Since problems from 30 chapters in Organic Chemistry have been answered, more than 286632 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • acetylide ion

    The conjugate base of acetylene or any terminal alkyne.

  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • alkali metals

    Members of group 1A in the periodic table. (Section 7.7)

  • benzylic position

    A carbon atom that is immediately adjacent to a benzene ring.

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • carbonyl group

    A CRO bond. carboxylic acid derivative (Sect. 21.6): A compound that is similar in structure to a carboxylic acid (RCOOH) but the OH group of the carboxylic acid has been replaced with a different group, Z, where Z is a heteroatom such as Cl, O, N, etc. Nitriles (R!C#N) are also considered to be carboxylic acid derivatives because they have the same oxidation state as carboxylic acids.

  • catalyst

    A substance that changes the speed of a chemical reaction without itself undergoing a permanent chemical change in the process. (Section 14.7)

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • crystal-field theory

    A theory that accounts for the colors and the magnetic and other properties of transition-metal complexes in terms of the splitting of the energies of metal ion d orbitals by the electrostatic interaction with the ligands. (Section 23.6)

  • dissolving metal reduction

    A reaction in which an alkyne is converted into a trans alkene.

  • exo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • frontier orbitals

    The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) that participate in a reaction.

  • Infrared (IR) spectroscopy

    A spectroscopic technique in which a compound is irradiated with infrared radiation, absorption of which causes covalent bonds to change from a lower vibration state to a higher one. Infrared spectroscopy is particularly valuable for determining the kinds of functional groups present in a molecule.

  • law of constant composition

    A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)

  • mean free path

    The average distance traveled by a gas molecule between collisions. (Section 10.8)

  • N-glycoside

    The product obtained when a monosaccharide is treated with an amine in the presence of an acid catalyst.

  • polarization

    For light, the orientation of the electric field.

  • polycarbonates

    Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons

  • Sanger dideoxy method

    A method developed by Frederick Sanger for sequencing DNA molecules