Tetraphenylcyclopentadienone Reaction Lab Report

Many sources of error were responsible for recovering a small amount of product. Introduction: The carbon-carbon bond formation is an important tool in organic chemistry to construct the simple as well as an organic compound. There are several

The goal of this experiment was to isolate three different molecules (acidic, basic, and neutral) from a mixture and identify their molecular structure. This was accomplished by using acid/base liquid extraction and H NMR analysis. The neutral component of the unknown mixture #191 was fluorenone. This was evident due to an H NMR spectra that had a high presence of hydrogen signals in the 7.2- 7.7 ppm range. Chemical shift values for fluorenone stated in the lab manual were 7.27, 7.47, 7.48, and 7.6 (CITE), indicating that the corresponding H NMR spectra for the neutral unknown is of this chemical.

Testing phase finds differences in positive/negative documents by the centroid obtained in training phase by ranking each of them. The simple way to estimate similarity between documents and centroid by summing weights of patterns which are in the documents. VII. Experimental Results To determine accurate measures of similarity or difference between documents you depict results by graph pattern and table pattern. The experimental setup consists of relevant documents that you termed as positive and negative documents .i.e

The goal of the experiment is to synthesize a bromohexane compound from 1-hexene and HBr(aq) under reflux conditions and use the silver nitrate and sodium iodide tests to determine if the product is a primary or secondary hydrocarbon. The heterogeneous reaction mixture contains 1-hexene, 48% HBr(aq), and tetrabutylammonium bromide and was heated to under reflux conditions. Heating under reflux means that the reaction mixture is heated at its boiling point so that the reaction can proceed at a faster rate. The attached reflux condenser allows volatile substances to return to the reaction flask so that no material is lost. Since alkenes are immiscible with concentrated HBr, tetrabutylammonium bromide is used as a phase-transfer catalyst.

Purpose The purpose of this lab was to measure the temperature of a solution to see how much energy was gained/lose during the reaction between the NiCl2 and Ethylenediamine. In this experiment we were also finding how many Ethylenediamine will bind to Ni+2 in an aqueous solution. By measuring the change in evolved heat, it’s possible to find the maximum number of Ethylenediamine molecules that have attached to each ion. Procedure Gather materials Analytic Balance Pasco with temperature probe Styrofoam cup Tape 5 M Ethylenediamine 0.998 M NiCl2 10 mL Pipet 2 mL

Flucloxacillin: - It is a member of the penicillin family that is used as an antibiotic for the staphylococcal infection (bacterial infection) that affects the human tissues of the skin and the lungs (pneumonia). It is also used in the treatment of food (rotten food) and poisoning of theblood. Staphylococcus may also be a risk to the human life if it releases its toxins by some strains of the bacteria to cause toxic shock. - Flucloxacillin is prescribed mainly in Australia & Europe, as it is very effective against the staphylococcus bacteria by inhibiting the synthesis of its cell wall then it will die. - Flucloxacillin is a ß-lactam antibiotic with a narrow spectrum.

Benzyne Formation and the Diels-Alder Reaction Preparation of 1,2,3,4 Tetraphenylnaphthalene Aubree Edwards Purpose: 1,2,3,4-tetraphenylnaphthalene is prepared by first producing benzyne via the unstable diazonium salt. Then tetraphenylcyclopentadienone and benzyne undergo a diels-alder reaction to create 1,2,3,4-tetraphenylnaphthalene. Reactions: Procedure: The reaction mixture was created. Tetraphenylcyclopentadienone (0.1197g, 0.3113 mmol) a black solid powder, anthranilic acid ( 0.0482g, 0.3516 mmol) a yellowish sand, and 1,2-dimethoxyethane (1.2 ml) was added to a 5-ml conical vial.

Hucknall, David 2012, Chemistry of Hydrocarbon Combustion, Chapman and Hall, London 2. University of California, 2014, Index of Hydrogen Deficiency, viewed 13 August 2017, https://chem.libretexts.org/Core/Organic_Chemistry/Fundamentals/Index_of_Hydrogen_Deficiency_(IHD) 3. Brown, William 2017, Organic Chemistry, Cengage Learning, Dallas 4. Chapman, Brian 2003, Organic Chemistry, Energetics, Kinetics and Equilibrium, Thomas Nelson, Cheltenham 5. Solomons, Graham 2004, Organic Chemistry, J. Wiley & Sons, Tampa 6.

The yellow solution containing the reactants was slowly poured into the beaker containing the cold water and the acid in order to cause the precipitation of the alcohol, 9-fluorenol and to destroy (hydrolyzed) the unreacted excess sodium borohydride. Subsequently, the white precipitate was vacuum filtered and washed twice with 20.0 ml portions of distilled cold water by pouring the liquid into the Buchner Funnel during filtration. It was necessary to wash the alcohol prior to recrystallization considering that the C-OH bond is easily broken by the formation of a stable and benzylic carbocation that favors the synthesis of difluorenyl ether. Finally, before the purification by recrystallization of the obtained product, the white solid alcohol was allowed to dry over a period of a

Experiment 12: Dehydrobromination Discussion In this experiment, a double elimination reaction was performed on meso-stilbene dibromide, to form diphenylacetylene by eliminating two hydrogen and two bromine atoms in he presence of potassium hydroxide. The product was filtered and identified by comparing melting point data, and percent yield was calculated. Since an E2 reaction was performed in this experiment, the ideal conformation for the hydrogen and bromine would have been anticoplanar. However, since the phenyl groups were bulky and the atom was not symmetric, the hydrogen and bromine could at best be antiperiplanar.

The possible explanations and changes to make are similar to the previous questions. Conclusion and Future Experiment 18. The identity of the product and unknown were 4-tert-butylbenzyl phenol ether and tert-butyl phenol respectively. The key to making this discovery was the melting point and TLC results!

It is understood the mechanism is acid-catalyzed where protons coordinate with the carbonyl oxygen to make the carbonyl carbon more electropositive for nucleophilic attack (Scheme 1). In the experimental procedure all reactants were added together, this is inefficient as the protons can coordinate with either trans-cinnamic acid or methanol. Coordination with methanol is unnecessary as it reduces its nucleophilicity and makes less protons available to coordinate with the carboxylic acid. To improve

C6H12 Possible side reactions: C6H6 + nH2 → cracking products C6H12 (benzene) ↔ C6H12 (methyl cyclo pentane) C6H6 + nH2 → C +

This was proved by utilizing the IR spectrum to verify the C =O was not in the final product as it lacked the 1640 cm-1 peak. The melting point of 113-115 degrees C proved that the final product obtained was the E-Stilbene. The TLC plate proved that the E and the Z product was produced, show cased by the double intensity of the DCM spot to the final product’s spot, both which had an Rf of 0.92. The double intensity proved that both products were produced, but through heating and filtering, the Z-Stilbene was

Bromination is a type of electrophilic aromatic substitution reaction where one hydrogen atom of benzene or benzene derivative is replaced by bromine due to an electrophilic attack on the benzene ring. The purpose of this experiment is to undergo bromination reaction of acetanilide and aniline to form 4-bromoacetanilide and 2,4,6-tribromoaniline respectively. Since -NHCOCH3 of acetanilide and -NH2 of aniline are electron donating groups, they are ortho/para directors due to resonance stabilized structure. Even though the electron donating groups activate the benzene ring, their reactivities are different and result in the formation of different products during bromination.