Solutions for Chapter 4.3: IUPAC Nomenclature of Alcohols

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 4.3: IUPAC Nomenclature of Alcohols

Solutions for Chapter 4.3
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This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 4.3: IUPAC Nomenclature of Alcohols includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 4.3: IUPAC Nomenclature of Alcohols have been answered, more than 10850 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • Allene

    The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.

  • base peak

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

  • charcoal

    A form of carbon produced when wood is heated strongly in a deficiency of air. (Section 22.9)

  • conformation

    A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.

  • conjugate acid

    A substance formed by addition of a proton to a Brønsted–Lowry base. (Section 16.2)

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • dipole-dipole interactions

    Theresulting net attraction between two dipoles.

  • Electrophilic aromatic substitution

    A reaction in which there is substitution of an electrophile, E1, for a hydrogen on an aromatic ring

  • Gibbs free energy (G)

    The ultimate arbiter of the spontaneity of a reaction, where DG = DH - T DS.

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • hydroxyl group

    An OH group.

  • intermetallic compound

    A homogeneous alloy with definite properties and a fixed composition. Intermetallic compounds are stoichiometric compounds that form between metallic elements. (Section 12.3)

  • ketose

    A carbohydrate that contains a ketone group.

  • mean free path

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

  • metal complex

    An assembly of a metal ion and the Lewis bases bonded to it. (Section 23.2)

  • nucleic acids

    Polymers of high molecular weight that carry genetic information and control protein synthesis. (Section 24.10)

  • oxidation state

    A method of electron book-keeping in which all bonds are treated as if they were purely ionic.

  • peptide bond

    A bond formed between two amino acids. (Section 24.7)

  • Retrosynthesis

    A process of reasoning backwards from a target molecule to a suitable set of starting materials.

  • reverse osmosis

    The process by which water molecules move under high pressure through a semipermeable membrane from the more concentrated to the less concentrated solution. (Section 18.4)

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