Provide the organometallic reagent that is needed to perform the transformation shown below. (Use the Reagent Cabinet List as a reference for correct formatting of your answer) OH
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- For the following reactions, two different products are formed based on the reaction conditions employed (1 and 2). Draw the mechanisms for the formation of both substitution products, using curvy reaction arrows and showing all important intermediates. Label each enolate intermediate as either kinetic or thermodynamic and provide all conditions and starting materials required for the reactions to occur.9. Need to check answers part1: image part 2;Select all that apply about the transformation above:Choose one or more:additionhydrationsubstitutionhydrogenationExamine the above reactions (RXN 1-6). Choose the letter of your answer from the choices provided. RXN 1 is completed by RXN 2 is completed by RXN 3 is completed by RXN 4 is completed by RXN 5 is completed by RXN 6 is completed by
- Steps 5 and 6 combined are best described as which of the following? 1. A reduction followed by reoxidation at C3 2. Two keto-enol tautomerizations that lead to stereochemical inversion at C3 3. An elimination followed by addition that leads to stereochemical retention at C4 4. Dehydration followed by hydration that leads to stereochemical retention at C4Why 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.a) Which of the following is a key intermediate for Step 1 of the reaction shown in the box? (image 1) b) please name the functional groups (image 2)
- Which reagent is required to complete the reaction in Figure 11? [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] * Your answerThis is about reaction of glycol. Pinacol rearrangement reaction 1. Find the mechanism of reaction.[IV1] Instructions: Follow the flow of electrons indicated by the curved arrows in each of the following reactions, and predict the products that result: (refer to the photo below)
- With the choice of thumbnails labeled A to P below, construct a comic strip depicting the complete mechanism of cyclopentane monobromination. List all the steps and in the correct order. Enter your answer as follows: ABCDEF (sequence of capital letters without spaces). N.B. There are more thumbnails than necessary.The reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followedWhich one of the compounds below is the major organic product of Reaction #1?