imagine that you were tasked with synthesizing100g of acetylferrocene using ferrocene
1. how would you use TLC to assist with maximizing the yield of the reaction
2.explain
1.
The conversion of ferrocene to acetyl ferrocene is monitored on TLC plate. The reaction is run till the starting material (ferrocene) is completely converted into product (acetyl ferrocene).
2.
On TLC plate, two samples are spotted, one is the starting material (ferrocene) and the other is the reaction mixture. The TLC plate is run at several points during the course of the reaction and the progress of the reaction is monitored.
Initally, only starting material is present in the reaction mixture. During the course of reaction, the intensity of the spot for the starting material in the reaction mixture decreases and the intensity of the product increases. At one time, no starting material can be seen in the reaction mixture. This shows the completion of the reaction.
imagine that you were tasked with synthesizing100g of acetylferrocene using ferrocene 1. how would you use...
imagine that you were tasked with synthesis 100g of acetylferrocene using the reaction (ferrocene under H3PO4 and Acetic anhydride to form acetylferrocene). 1. how would you use TLC to assist with maximizing the yield of the reaction 2. explain it
Synthesis and Purification of Acetylferrocene: 1.Where on the ferrocene molecule was the second acetyl group added? Explain why this position is favored on the molecule. 2.Explain why ferrocene has a higher Rf value on silica gel TLC than acetylferrocene.
These questions are from an experiment where we had a mixture of Ferrocene, acetylferrocene and diacetyl ferrocene and we separated each by using column chromatography. Before doing the column chromatography we did TLC analysis to ensure that we did, in fact, have a mixture of these 3 compounds. During the column chromatography we first eluted the ferrocene using pure hexane. Then we eluted the acetylferrocene using a 1:1 mixture of hexane and methylene chloride. Then we eluted the diacetylferrocene using...
Questions: vide the mechanism of the synthesis of (1.) acetylferrocene, .) 1-1'diacetylferrocene from; Acetic Anhydride, Ferrocene, and ! inydride, Ferrocene, and Phosphoric Acid. Determine the % yield of 1-acetylferrocene if you st excess acetic anhydride. Acetylferrocene is the only product in this case U OT I-acetylferrocene if you started with 300 mg. of Ferrocene and Uraw structures of all starting reagents and all potential products of this reaction,
Friedel-Crafts Acylation of Ferrocene "riedel-Crafts reactions are examples of electrophilic aromatic substitution reactions. The eaction involves the substitution of hydrogen on the aromatic ring system by an electrophilic arbon species forming a new carbon-carbon bond. Friedel-Crafts reactions may be used to ntroduce either an alkyl or acyl group. Ferrocene does not undergo addition reactions typical of cyclopentadiene, but undergoes Electrophilic aromatic substitution. The Friedel-Crafts acylation reaction of ferrocene involves he addition of the acylium cation to one of the carbon...
If you were tasked with starting a new healthcare clinic, would you lean toward using the cash or accrual method of accounting? Why? How would revenue recognition and expense-matching principles be related to your decision.
Imagine that you are on a team that that has been tasked with creating an online course delivery system. One of your coworkers wants to model the entire course in UML. Another coworker disagrees with the use of UML and would rather use pseudocode exclusively. Analyze both strategies and suggest at least two (2) major benefits of using UML as well as two (2) major benefits of using pseudocode. Recommend the approach you would suggest in the given scenario and...
Acetylation of ferrocene and column chromatography
Lab 4: Question 3 Homework • Unanswered Important ... The solvent is changed from petroleum ether to diethyl ether after the ferrocene is collected from the column. Why not use diethyl ether the entire time? Because diethyl ether is more polar than petroleum ether Because petroleum ether selectively elutes ferrocene since it contains more ether oxygens than diethyl ether Because diethyl ether would lead to a poorer separation of ferrocene and acetylferrocene Both a...
1. What are the main differences between thin layer chromatography (TLC) and column chromatography (CC)? 2. Are CC and TLC operations conducted concurrently? Explain. 3. Name a few packing materials used in packing columns in Column Chromatography operations. 4. Explain the role of eluting solvent(s) in column chromatography procedures. 5. When performing column chromatography, which of the following compounds would you expect to elute first: Ferrocene of acetylferrocene? Explain why.
betal Question 9 1 pts If you are given a mixture of three compounds like you were given in lab with the acetylferrocene/ferrocene mixture), what would be the proper order to separate and isolate those three compounds. 1st step Choose Run the column, collecting fractions in tared flasks Run a TLC of the three compounds in a fairly non-polar solvent such as hexanes Once the best eluent has been found, build a column using that event If the compounds are...