Grignard Reagent Lab Report

The data observed and recorded in this lab shows that the concentration of miracle gro’ does affect the growth rate and germination speed of black eyed peas. The data is shown through two graphs and two data tables. The control group in this experiment is the seeds with a 0% concentration of miracle gro’, therefore the seeds with just water. The experimental groups are different concentrations of miracle gro’ including a 10%, 15%, 20%, 25%, and 30% concentration. The variable in this experiment is the amount/concentration of miracle gro’.

In this lab, three unknown compounds were separated from a mixture and identified by melting point. Unknown mixture #124 has components of acid, base and neutral compound. The compounds were identified by melting point and matched up with the known melting points from a given list. In order to identify the compound it was important to separate by dissolving the mixture in an organic solvent which was not soluble in water, and then extracting the solution first with HCl, and then dilute sodium hydroxide solution. From the separation mixture, the aqueous layer were obtained and labeled as TT-1 (base), TT-2(acid) and TT-3 (neutral) in three different test tubes for later recovery.

The purpose of this laboratory experiment was to react methyl benzoate with nitric acid and identify the position of the substituted nitro group in the final product molecule. Methyl benzoate was added to cool concentrated sulfuric acid in order to amplify the directing effect of the nitro group addition, such that without the sulfuric acid the protonation would have happened at the carbon oxygen double bond. The mixing of concentrated nitric acid with concentrated sulfuric acid was to achieve Reaction 1 from Table 1, formation of the nitronium ion. Both of these reactions were kept at temperatures around 0°C, since they are exothermic reaction and presence of heat could lead to production of unnecessary dinitro by-products.

The purpose of this experiment was to learn about metal hydride reduction reactions. Therefore, the sodium borohydride reduction of the ketone, 9-fluorenone was performed to yield the secondary alcohol, 9-fluorenol. Reduction of an organic molecule usually corresponds to decreasing its oxygen content or increasing its hydrogen content. In order to achieve such a chemical change, sodium borohydride (NaBH4) is used as a reducing agent. There are other metal hydrides used in the reduction of carbonyl groups such as lithium aluminum hydride (LiAlH4).

The next part of the experiment, alkyl halide classification tests, will be used to determine the degree of substitution of the alkyl halide that was formed during the reaction. For this experiment specifically, this allows for the verification of the formation of a primary bromoalkane from the primary alcohol. The success of the experiment will be determined by a percent yield, analysis of the infrared spectroscopy reading, and the results of the alkyl

Bromination is the process where an alkene is halogenated with bromine. The purpose of this experiment was bromination of stilbene to stilbene dibromide. The element bromine is toxic and requires maximum care when used. Bromine was generated in the reaction mixture by using a green method. Less hazardous reagents were used to do so.

The Wittig reaction is valuable reaction. It has unique properties that allows for a carbon=carbon double bond to form from where a C=O double bond used to be located. Creating additional C=C double bonds is valuable due to its use in synthesis. The Wittig reaction will allow the synthesis of Stilbene (E and Z) from a Benzaldehyde (Ketcha, 141).

Verna Wang Hannah Palmer CHEM 101-069 Lab 11-19-16 Stoichiometry and Limiting Reagents Lab Report Purpose: We are using the reaction of sodium hydroxide and calcium chloride to illustrate stoichiometry by demonstrating proportions needed to cause a reaction to take place. Background: Just like a recipe would call for a specific amount of one ingredient to a specific amount of another, stoichiometry is the same exact method for calculating moles in a chemical reaction. Sometimes, we may not have enough of or too much of one ingredient , which would be defined as limiting and excess reagent, respectively.

MSc FOOD BUSINESS MANAGEMENT AND TECHNOLOGY Food Formulation & Processing Laboratory Practical Submitted to, Submitted by, Janis Kelly Blesson Abraham Mathew PRACTICAL NO- 3 SEPARATION OF AMINO ACIDS BY THIN LAYER CHROMATOGRAPHY Chromatography Chromatography is a technique that is used to separate two or more different

The objective of this lab was to determine the activating strengths of the directing groups in aniline, phenol, acetanilide and anisole by using melting point to identify the products of their electrophilic aromatic bromination reactions with pyridinium tribromide in glacial acetic acid. The amount of substitution in an aromatic compound in a electrophilic aromatic bromination reaction is dependent upon the reactivity of the aromatic compound itself, which is determined by its substituents’ inductive effects. In the case of this experiment, four different aromatic compounds were used, containing either -NH2, -OH, -OCH3, and -NHCOCH3 as substituents. Of these four, the most activating substituent is -NH2 in aniline because nitrogen is less electronegative than the oxygens in -OH and -OCH3 in phenol and

INTRODUCTION Gadolinium is a shiny silvery white, malleable, ductile, metallic, rare earth element which is located in group 3, f-block, period 6 and classified in the series of lanthanides in the elements of periodic table and has 27 isotopes whose half-lives are known with mass numbers from 137 to 164. This element is considered a rare earth element because there is such a small amount of it, and it is not found often in its simplest form. It was discovered in 1880 by Jean Charles de Marignac where it was extracted in from the mine located in Ytterby in Sweden, but it was isolated from metal oxide in 1886 by Lecoc de Boisbaudran who named it after the Finnish Chemist Johan Gadolin who discovered the first rare earth element in 1794. Gadolinium

Typically, due to the dual reactivity of organosilane, both alkoxy group (OR\) and non-hydrolysable organic moiety (X), it is used to couple inorganic or organic substrates such as minerals, metals or cellulose and polymeric matrices such as rubber, thermoplastic or thermosets to improve its physical properties. The applications include adhesion promoter, dispersing/hydrophobing agent and crosslinking agent. 1.3.1 Adhesion Promoter Organosilanes are effective adhesion promoters when used as integral additives or primers for paints, inks, coatings, adhesives and sealants. As integral additives, they must migrate to the interface between

4- They highly reactive with amines, alcohols, acetylene and water. 5- They may react with the compounds which contain hydrogen that should be active as well as, halogen and carbonyl compounds. Reactions of Grignard

117(35): p. 8999-9002. 6. Fukuzawa, S.-i., et al., Samarium(II) Triflate as a New Reagent for the Grignard-Type Carbonyl Addition Reaction.

In this experiment, extraction was used as a separation technique to separate the acid, base, and neutral compounds. In extraction, two immiscible solvents with opposite polarities are used to dissolve different parts of the solute with different polarities, so they form two distinct liquid layers. In this experiment, methanol, an organic solvent, and an aqueous solution were used as the two immiscible solvents. The extraction solvent must also be capable of dissolving one of the mixture components. While initially it seems as though methanol, an organic solvent would be incapable of dissolving a polar acid or base, the conjugate of the acidic and basic compound will dissolve in methanol.