The purpose of this experiment of this experiment is to create Malachite green or crystal violet by first preparing a Gringard reagent, and then reacting it with methyl benzoate. The Gringard reagent was formed from 4-bromo-N,N-dimethylaniline. In the second part of the lab we reacted the Gringard reagent with diethyl carbonate to form crystal violet.
Why would submitting a NMR sample of your dye solution (not the pure dye compound itself) be unlikely to provide a useful spectrum?
The purpose of this experiment of this experiment is to create Malachite green or crystal violet...
What is the reaction drawn out for the synthesis of malachite green and crystal violet using methyl benzoate for malachite green and diethyl carbonate? grignard reagent was 4-bromo-n-n-dimethyl aniline magnesium bromide, also please show reaction of forming this reagent using 4-bromo-n-n-dimethylaniline, anhydrous tetrohydrofuran and magnesium turnings.
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...
Post Lab Questions: CI MALACHITE GREEN CRYSTAL VIOLET 1. Why does the malachite green dye elute first? What physical properties does it have that affect it's interaction with alumina and how are those different from crystal violet? 2. Write the reaction of crystal violet with 1 equivalent of HC. 3. Why does adding HCI cause crystal violet to elute more quickly? What changes with it's physical properties and how does that property affect it's interaction with alumina?
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.
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...
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....
Grignard Reaction with a Ketone: Triphenylmethanol Introduction: The purpose of this lab is to prepare phenylmagnesium bromide, a Grignard reagent, and react it with benzophenone to give triphenylmethanol. Grignard reagents are very reactive and must be synthesized in an environment free of water or any other source of potential proton donor. Once made, the Grignard reagent will do a nucleophilic attack on the carbonyl carbon of the ketone, benzophenone. The result is an alkoxide that is then protonated to give...