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Textbooks / Chemistry / Organic Chemistry, - Standalone Book 2

Organic Chemistry, - Standalone Book 2nd Edition - Solutions by Chapter

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Organic Chemistry, - Standalone Book | 2nd Edition - Solutions by Chapter

This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. Since problems from 27 chapters in Organic Chemistry, - Standalone Book have been answered, more than 117767 students have viewed full step-by-step answer. The full step-by-step solution to problem in Organic Chemistry, - Standalone Book were answered by , our top Chemistry solution expert on 01/19/18, 05:12PM. This expansive textbook survival guide covers the following chapters: 27.

Key Chemistry Terms and definitions covered in this textbook
  • carbohydrates

    Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • corrosion

    The process by which a metal is oxidized by substances in its environment. (Section 20.8)

  • crossed aldol reaction

    An aldol reaction that occurs between different partners.

  • crystalline solid (crystal)

    A solid whose internal arrangement of atoms, molecules, or ions possesses a regularly repeating pattern in any direction through the solid. (Section 12.2)

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • dilution.

    A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • enol

    A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.

  • Ether

    A compound containing an oxygen atom bonded to two carbon atoms.

  • fibers

    Strands of a polymer that are generated when the polymer is heated, forced through small holes, and then cooled.

  • 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.)

  • 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.

  • metallic solids

    Solids that are composed of metal atoms. (Section 12.1)

  • molecular compound

    A compound that consists of molecules. (Section 2.6)

  • Pro-R-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an R confi guration

  • 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.

  • renewable energy sources

    Energy such as solar energy, wind energy, and hydroelectric energy derived from essentially inexhaustible sources. (Section 5.8)

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

  • SN1

    A unimolecular nucleophilic substitution reaction.