What is the reaction drawn out for the synthesis of malachite green and crystal violet using...
Write the mechanism for the formation of Malachite Green from methyl benzoate. Be sure to show all steps, including the loss of water. 1. 2. Write the mechanism for the formation of Crystal violet from diethyl carbonate. 3. Methyl benzoate is an ester, but is technically a carboxylate ester. Diethyl carbonate is a 4. Why is the green dye in this experiment called "Malachite Green"? Hint: Try looking in a 5. Write the balanced equation for the reaction of hydrochloric...
1. Choose one of the two dyes prepared from this lab and write out its complete mechanism. Assume the Grignard reagent has already been formed. 2. (a) What would happen to the color of your dye if you added sodium hydroxide to the solution until the pH reached 10? Why? (b) Show a mechanism from this reaction. For malachite green: Weigh 0.105 g of methyl benzoate into a small clean vial. Add 1 mL anhydrous tetrohydrofuran to the vial. For...
can you please answer both of these questions. the dyes are crystal violet and malachite green Choose one of the two dyes prepared from this lab and write out its complete mechanism, Assume the Grignard reagent has already been formed (a) What would happen to the color of your dye if you added sodium hydroxide to the solution until the pH reached 10? Why? (b) Show a mechanism from this reaction. 1. 2.
Write balanced reaction equations separately for each of the four steps of your reaction (just give the balanced overall equation, not mechanisms). Include all counterions and side products as well as the major reactants and products. a. formation of the n-butyl bromide Grignard reagent b. Magnesium-halogen exchange reaction to make the 4-bromo-N,N-dimethylaniline into a Grignard reagent c. reaction of the Grignard reagent with methyl benzoate. Do not include the addition of HCl step yet. d. reaction of the product in...
i need help with the prelab questions please Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
1. Write equations for the reaction of 2-methyl propane-1- magnesium bromide with acetaldehyde include the hydrolysis of the reaction mixture with dilute acid. B) Why should anhydrous diethyl ether be used rather than regular solvent grade diethyl ether to prepare the solution of benzaldehyde that is added to the Grignard reagent, 2- methyl propane-1- magnesium bromide? C) By drawing the structure indicate the polarity (charge separation) of the bond between carbon and bromine in 1-bromo-2-methyl propane. Is 1-bromo-2-methyl propane electrophile...
S RROwn as nucleophilic addition. The C-O bond is highly polarized, making carbonyl compounds electrophilic at carbon. If the Grignard reagent reacts with an aldehyde, ketone or ester, the ultimate product is an alcohol. Overall Reaction 0 Br Me PartA Part B Pre-lab questions (15 points) Show the mechanism of the reaction of bromobenzene with magnesium metal in anhydrous diethyl ether There are many inert solvents that could be used but diethyl ether was chosen because it can assist the...
i need help with the postlab questions please Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
A Grignard reaction was performed using the following steps: Step 1: Addition of Grignard Reagent: Phenyl Magnesium Bromide a solution of phenyl magnesium bromide (2.7 mL of a 3.0 M solution in anhydrous diethyl ether) and 5 mL of anhydrous diethyl ether was dispensed into the round-bottom flask and stirred with a stir bar. Step 2: Addition Formation: Reaction with Benzophenone A solution of 0.72 g (mp = 48-49 degrees C) of benzophenone and 2.0 mL of anhydrous diethyl ether...
Green synthesis of Chalcones: we carried out a reaction of green synthesis of chalcones using 4-methylacetophenone and 4-methylbenzaldehyde. Ideally we should have used 5 mmol for each, but we used 0.6 ml of 4-methylacetophenone and 0.5ml of 4-methylbenzaldehyde. Draw the complete reaction of this experiment, and show what is the limiting reagent that should be used to calculate percent yield.