Write an introduction on the ferrocene molecule, describing it's structure. What would happen if ferrocene was acetylated. Discuss the two products that may be formed due to the attachment of the acetyl group. Draw this in a reaction mechanism.
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Write an introduction on the ferrocene molecule, describing it's structure. What would happen if ferrocene was acetylated. Discuss the two products that may be formed due to the attachment of the acetyl group. Draw this in a reaction mechanism.
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- For the substitution reaction. Draw the structure of the intermediate that forms in the rate determining step. Он HBr (aq) BrDesribe the reaction product.Cinnamon is made up of a mixture of many compounds. Cinnamaldehyde is the component responsible for cinnamon flavor. Several of these compounds are also a potent antimicrobial compounds present in essential oils. The following results were obtained for known concentrations of three of the compounds. Concentration (mg sample/200 uL) Cinnamaldehyde Eugenol Thymol 0.50 0.4 0.65 1.8 0.75 1.0 0.8 1.10 1.2 1.25 2.0 1.30 3.0 1.50 1.5 1.90 3.1 2.0 4.6 2.50 4.0 5.8 Determine the calibration curve equations for each component including regression. which component has the highest calibration sensitivity? A sample containing the three essential oils in part b gave the peak areas relative to the internal standard of cinnamaldehyde 2.6, eugenol 0.9 and thymol 3.8. Determine the concentration of each of the oils in the sample and the standard deviations.
- The following elimination reaction results in a mixture of products. Explain why the major products obtained in larger quantities than the minor products. Use chemical structures as necessary to justify your answer.Write an equation for the reaction of chloroacetic acid (Ka=1.5103) with trimethylamine (Kb=5.9105) . Calculate the equilibrium constant for the reaction. If 0.10 M solutions of these two species are mixed, what will be their concentrations at equilibrium?7. a) Complete the two reactions below. Provide full chemical reactions with structures and names of reactants and all products. Include necessary catalysts. b) What type of reaction is it? N-ethylprobutanamide + H₂O → What type of reaction is this? Drawings: (product names)
- The extraction could have been performed using aqueous sodium bicarbonate (NaHCOs) instead of aqueous sodium hydroxide. If this had been attempted, there may have been problems with the procedure. i.Write the balanced equation which occurs when benzoic acid reacts with sodium bicarbonate to form a gaseous product (among other things).20:32 hydroxide 2. Using curved arrows, show the deprotonation mechanism of phenol with (OH). Also, provide the structure of the product of this deprotonation. Start answering this question by drawing the structure of phenol. Then hydroxide ion. Find your most reactive electrons and draw the curved arrow that shows where they would go to deprotonate phenol. Then "make a bond break a bond" write they question 3. Provide valid resonance structures for the product of the previous arrow(s) charge moving onto the ortho- and para positions. Use curved to show how the charge resonates to the next structure in your scheme. all the proper notations for depicting resonance. that show the in the structures Be sure to use Send a chat CPotassium permanganate and potassium dichromate are very similar in their oxidizing abilities, however there are differences. If I want to convert 4-hexen-1-ol into 4-hexenoic acid, which would be the appropriate oxidizing agent to use? Explain your answer using equations that show the two different products that would form via the two different oxidizing agents.
- CHEMISTRY AND ENVIRONMENTAL POLLUTION Explain how Hg2+ ion is transformed into methylmercury anddimethylmercury in the aquatic environment.Give the oxidation products of the following reactionsn-Butylamine is made by reaction of O cyanide, followed by reduction with lithium aluminum hydride. azide, followed by reduction with lithium aluminum hydride. ammonia, followed by addition of base. ammonia, followed by acidification.