GS Q5 Show all missing reagents and intermediates in the reaction sequence below. Put the information in the appropriately labelled box on the GradeScope template. EtO. (C) Heat CO2Et + (A) (B) Ph3P=CHCO,Et (2 equiv) (D)
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- I want the sequence of the reaction to get to the target for number 3 thank uPredict the product of the reaction below. Use curved arrows to show the reaction mechanismYou react an unknown aldehyde (substitutent group marked with an "x") with a ketone and get the product on the right (substitutent group still unknown). HNMR data for the product is shown below. Which of these 3 aldehydes is the reactant that was used? sorry the HNMR looks rough, this was the last question on my final and I am still kinda reeling from it.
- Can you help me get the missing products. Drawn out in extended form please?This question refers to the following reaction: (SEE IMAGE BELOW) i) Determine whether the main reaction to form F is a substitution or an elimination reaction. Explain your choice in no more than two sentences. ii) Draw the structure of the product F. iii) What is the mechanism of the above reaction (i.e. SN1, SN2, E1 or E2)? Explain your choice in one sentence based on your answer in (i) above. iv) Using curly arrows show the mechanism for the reaction to give F.Show the Reaction of a 1° ROH with HX—An SN2 Mechanism ?
- exolain how to solve trial one so i can do the remaining trials on my own. thanksWhy we need step 3 before step 4? a. Because the nitro group increases the electrophilicity at the ortho positions which is where the bromine is added. b. Because the amine group is a strong ortho, para director which is what controls the regiochemical outcome of this bromination. c. Step 4 is unessesary. The symmetry of compound 3 allows for the bromination to be regioselective and give compound 5. 5. There will be a mixture of products because there is no selectivity for a major product.Draw the molecule: Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur simultaneously and compete with each other.Show what products might be expected from the reaction of 2-bromo-3-methylbutane (a moderately hindered 2∘∘ alkyl halide) with sodium ethoxide. Do not worry about sterechemistry inther SN2 product for this problem. Don't forget about stereochemistry.