Sample Test Question

Draw the starting materials needed (in the presence of LDA) to prepare this compound.

Step 1. Identify the alpha and beta carbons adjacent to the carbonyl group.

Step 2. Break the C-C bond between the two carbons

Answer: A carbonyl compound and an enolate is required to make this compound

Seminar Critique

The topic of this chemistry seminar was the affects of tobacco smoke on unborn children. Led by Dr. Steven Myers, the effects of tobacco, and the various adverse affects it has on the the development and well being of a unborn fetus as well as a newborn child were described. Dr. Myers is a faculty of University of Louisville Medical School and specializes in the Pharmacology/Toxicology department.

Prior to attending this seminar, I was much aware of the negative affects cigarette smoke had on a pregnancy, but after attending, the depth of my knowledge greatly increased. The various chemical found in cigarette smoke were discussed during the seminar. Dr. Myers described how the increased concentrations of these chemicals in the vicinity of a developing fetus can increase the likelihood of defects in the child. These abnormalities include, but are not limited to, cardiorespitory defects, neurological problems and SIDS (sudden infant death syndrome). One such chemical, 4-aminobiphenol, is particularly hazardous. As stated by Dr. Myers, it one of the most carcinogenic compounds known.

Molecular Weight: 169.22
Melting Point: 55 deg.C
Boiling Point: 302 deg.C

Hell-Volhard-Zelinsky Halogenation

The Hell-Volhard-Zilinsky Halogenation is a reaction in which the alpha carbon of a carboxylic acid is halogenated. This reaction is catalyzed by a necessary amount of PBr2, which replaces the OH, thus forming an acid bromide. The acyl bromide then tauteramerizes to form an enol. A molar amount of Br2 is also added, which bonds to the alpha carbon. This reaction differs from other halogenations in that it does not include a halogen carrier. The general reaction scheme of a Hell-Volhard-Zelinsky Halogenation is illustrated below.



A reaction involving the Hell-Volhard-Zelinsky Halogenation is the synthesis of 2-bromobutanoic acid, also called 2-bromobutyric acid, from butanoic acid.

Formula: C4H7BrO2

Molecular Weight: 167 g/mol

Melting point: -4 deg C

Boiling point 101 deg C

A reaction scheme of this reaction is illustrated below.

References:

http://en.wikipedia.org/wiki/Hell-Volhard-Zelinsky_halogenation

http://www.colvir.net/prof/carl.brabant/Faidherbe/acides.htm

Propyl Acetate

Propyl Acetate is a common solvent used as a flavoring due to its fruity taste. It is colorless and emits the odor similar to pears. Propyl acetate has a 2% water solubility and is miscible in most organic compounds. The structure and mass spectrum for Propyl Acetate is represented below.

Molecular Formula: C5H10O2 

Boiling Point: 216 deg. F (102 deg. C)
Freezing temperature of -139 deg F ( -95 deg C).
Density: .888 g/cm^3
Molecular Weight: 102.131 g/mol

Propyl acetate is formed by the esterifcation of acetic acid and 1- propanol by means of Fischer/Speier esterification.

My search for a reaction dealing with the conversion of propyl acetate into a carboxylic acid yielded no results, I did find some reaction involving propyl acetate used in distillation, though no carboxylic acids were formed. I searched the organic synthesis website supplied by Dr. Mullins and still had no luck, if any such reaction could be found by anyone, it would be much appreciated.

Thank for reading!!

Sources:

http://en.wikipedia.org/wiki/Propyl_acetate

http://msds.chem.ox.ac.uk/PR/propyl_acetate.html



Grignard Reaction

Our assignment this week was to locate a reaction containing either a organolithium, organocuperate or grignard reagent. I chose one containing the Grignard reagemt. A Grignard reagent is an alkyl or aryl magnesium halide that acts as a nucleophil and attatcks a electrophilic carbon that are polar bonded to another carbon atom.The reacton I chose was the synthesis of N,NDIBENZYL-N-(2-ETHENYLCYCLOPROPYL)AMINE.

This reaction involves the reaction of N,N - dibenzylformamide (in red) with the grignard reagent,  3-butenylmagnesium bromide (in green). The Grignard reagent is added dropwise for 30 minutes resulting in a temporary black precipitate which requires a stirring for an additional hour.

The resulting product,  N,N-Dibenzyl-N-(2-Ethenylcyclopropyl)Amine, results in the formation of two new C-C bonds (shown in yellow) forms a three carbon ring. The resulting product is a yellow silicon gel.