Phenyl Grignard Addition To Benzophenone Lab Report
Marissa De la Paz 29 October 2015 Landstrom T/R, 8am Experiment 13B: Phenyl Grignard Addition to Benzophenone The objective of this experiment is to first generate a Grignard reagent, then use that to synthesize triphenylmethanol. The Grignard reagent is necessary to create a new C—C bond. The formation of triphenylmethanol is broken down in several steps. Magnesium is added to a capped and dried flask with a crystal of iodine, ether and a drop of 1,2-dibromoethane. The iodine was essential to activate the magnesium. Ether was used as the solvent because there are no acidic hydrogen’s on ether that can potentially react with the Grignard reagent and also because ether has two lone pairs on the oxygen that can help to stabilize the magnesium
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Dihydroxyphenylalanine Lab Report
284 Words | 2 PagesEnzymes are an important part of the cell and are crucial to sustaining a healthy life for an organism. An enzyme is a protein, composed from amino acids, and an enzyme’s role in the cell is to increase the cell’s ability to perform chemical reactions (Brain 2000). The chemical reactions that cells perform are critical to the development of cells and are how cells grow (Brain 2000). Tyrosinase is an enzyme that is commonly found in plants, and its function is to cause plants to brown, a process known as melanization (Chang 2012). Dihydroxyphenylalanine (DOPA) is an amino acid that reacts with Tyrosinanse, and this reaction eventually leads to create melanin, a product of melanization (Waite 1991).
Grignard Reagent Lab Report
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1039 Words | 5 PagesThe 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!
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