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  2. Organic Nomenclature Problems - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/Questions/Nomencl/nomencl.htm

    Question 4: Nomenclature of Aromatic Hydrocarbons; Question 5: Nomenclature of Halogen Compounds; Question 6: Nomenclature of Alcohols; Question 7: Nomenclature of Aldehydes & Ketones; Question 8: Nomenclature of Carboxylic Acids. If you are asked to write a IUPAC name for a compound, pay careful attention to the syntax of this nomenclature system.

  3. Organic Chemistry Practice Problems at Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/Questions/problems.htm

    Organic Chemistry Practice Problems at Michigan State University. The following problems are meant to be useful study tools for students involved in most undergraduate organic chemistry courses. The problems have been color-coded to indicate whether they are: 1. Generally useful, 2.

  4. Organic Nomenclature - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/nomen1.htm

    The IUPAC nomenclature system is a set of logical rules devised and used by organic chemists to circumvent problems caused by arbitrary nomenclature. Knowing these rules and given a structural formula, one should be able to write a unique name for every distinct compound. Likewise, given a IUPAC name, one should be able to write a structural ...

  5. Nomenclature Examples - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/nomexmp1.htm

    Examples of the IUPAC Rules in Practice Illustration 1. CH 3 (CH 2) 2 CH(CH 3)CH 2 CH 3. When viewing a condensed formula of this kind, one must recognize that parentheses are used both to identify repeating units, such as the two methylene groups on the left side, and substituents, such as the methyl group on the right side.

  6. Nomenclature-Amines - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/Questions/General/amine1.htm

    This script written by William Reusch, Dept. of Chemistry, Michigan State University. Please send comments and corrections to whreusch@pilot.msu.edu.

  7. Virtual Textbook of Organic Chemistry - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/intro1.htm

    Concerning Practice Problems. The practice problems provided as part of this text are chiefly interactive, and should provide a useful assessment of the reader's understanding at various stages in the development of the subject. Some of these problems make use of a Molecular Editor drawing application created by Peter.Ertl.

  8. Chapter 23 Chemistry of Coordination Compounds - Michigan State...

    www2.chemistry.msu.edu/courses/cem151/chap24lect_2019.pdf

    Father of coordination chemistry First inorganic chemist to win Nobel Prize •suggested in 1893 that metal ions have primaryand secondaryvalences. ØPrimary valence equals the metal’s oxidation number ØSecondary valence is the number of atoms directly bonded to the metal (coordination number) Co(III) oxidation state Coordination # is 6 Cl-

  9. Organic Nomenclature Problems - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/Questions/Nomencl/nomencl2.htm

    If you are asked to write a IUPAC name for a compound, pay careful attention to the syntax of this nomenclature system. For example, commas and dashes must be used in precisely the correct manner, and extra spaces must be avoided. Spelling must also be absolutely correct.

  10. Chemistry of Amines - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/amine1.htm

    Practice Problems; The following problems review many aspects of amine chemistry. The first three questions concern the nomenclature of amines. The fourth focuses on the relative basicity of small groups of amines. The fifth requires that you choose reagents for accomplishing some multistep transformations.

  11. Nomenclature Examples - Michigan State University

    www2.chemistry.msu.edu/faculty/reusch/VirtTxtJml/nomexmp2.htm

    Examples of the IUPAC Rules in Practice. When one substituent and one hydrogen atom are attached at each of more than two positions of a monocycle, the steric relations of the substituents may be expressed by first identifying a reference substituent (labeled r) followed by a hyphen and the substituent locator number and name.