Grignard synthesis of triphenylmethanol lab report

In the event that water was able to settle along the apparatus, the yield of triphenylmethanol available after the completion of the Grignard reaction was probably less than expected. The yield of the product in the experiment is 1.

Saturated NaCl solution Methods: The presence of water in the process of generating Grignard reagent will causes the particular reagent to be decomposed. Procedure Into a dry 20 mL round bottom flask.

The chemical reaction between magnesium and bromobenzene is Grignard synthesis of triphenylmethanol lab report in below: The melting point of the final pure product was determined to be — During the experiment, there could have been more precaution taken to ensure that the reaction was free of water.

The reaction was refluxed to form the Grignard reagent and then recrystallized to obtain a pure product. In this stage, some white solid were precipitated out in the cold solution, the white solid is the desired product.

Avoid the diethyl ether from any heat source since it is extremely flammable. So, the solvent used in the experiment must not contain any water such as diethyl ether since it is a water free solvent.

If necessary, add more diethyl ether to the solution. Also, upon obtaining the melting point of the product, it was observed that the melting point range of the product was The sonicator is used to produce ultrasonic wave in which helps to remove the oxide coating physically.

Triphenylmethanol was synthesized with a 9. The amber colored solution became a darker brown, then changed to a pink color, and finally changed to a peach color.

Before beginning the experiment, wrap the glassware involved in aluminum foil and place the glassware in an oven to ensure that the glassware is dry and free of water. Aqueous layer was re extracted in the funnel.

Using the Grignard Reaction to Prepare Triphenylmethanol

The nucleophilic addition of Grignard reagent to methyl benzoate caused the methoxide became the leaving group from the intermediate and the formation of benzophenone. The formation of Grignard reagent is an exothermic process.

Calculate the percent yield of the product. When the reaction has been initiated, the appearance of bubbles on the solvent surface indicated that the formation of phenylmagnesium bromide start to occurr.

Obtain an IR spectrum of the product and analyze the peaks. Transfer the rinse solution from the round-bottom flask into the 5 mL conical vial used in the previous step. Make sure that the product is completely dried.

The formation of Grignard reagent is solvated by diethyl ether which protects the reagent from attacked by water molecules. The bromobenzene is reacted with magnesium metal to form phenylmagnesium bromide which is known as Grignard reagent.

Combine this rinse with the other rinses in the 50 mL Erlenmyer flask. The adding of diethyl ether in the mixture is works for the similar function which make sure the solvent is free from water.

The calcium chloride acts as a drying agent which to absorb all the water from the air in the reflux apparatus and it prevent the atmospheric moisture.

Using a clean filter-tip pipette, transfer the biphasic mixture from the round-bottom flask to a clean, dry 5 mL conical vial. Observe the biphasic clear mixture of organic diethyl ether layer at the top and the acidic aqueous layer at the bottom of the reaction mixture. This deviation may be due to the product is not completely dry so that it affects the melting point of the product.The Grignard Synthesis of Triphenylmethanol Organic Chemistry Lab II March 19, Abstract The purpose of this experiment was to synthesize the Grignard reagent, phenyl magnesium bromide, and then use the manufactured Grignard reagent to synthesize the alcohol, triphenylmethanol, by reacting with benzophenone and protonation by H3O+.

Triphenylmethanol Johnson, Chad Philip; T/Th Lab, am Submitted March 29th, Introduction The preparation of a Grignard reagent is an important laboratory technique and is a required. A Student Researched Lab Analysis of the Synthesis of Triphenylmethanol from Benzophenone and Bromobenzene.

Using this Grignard reagent, triphenylmethanol can be synthesized in a two-step reaction first adding the reagent and then adding an acid. Join our weekly lab-report contest for a chance to win cool prizes! View Lab Report - Organic chemistry lab report- Grignard's reaction from CHEMISTRY 12 at National University of Singapore.

Aim: Synthesis of Triphenylmethanol from benzophenone via Grignard%(3).

Grignard Synthesis of Triphenylmethanol Lab Report

Grignard Synthesis of Triphenylmethanol Lab Report A Grinded reagent is a type of ergonomically, which consists of a bond twine a metal and a carbon. There are three types of carbon-metal bonds: ionic, polar covalent, and covalent. Triphenylcarbinol: A Grignard Synthesis Chemistry L/L October 1, Laura Meraz.

2 Purpose: In this experiment, phenyulmagnesium bromide (a Grignard reagent) was prepared and used to produce triphenylcarbinol (a tertiary alcohol) by reacting with methyl benzoate.

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Grignard synthesis of triphenylmethanol lab report
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