2.) Predict the one major organic product (not side-products) for each of the following reactions. cold DMSO 0= S: heat DMSO 3.) Predict the products (including side-products) of the following reactions.
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![2.) Predict the one major organic product (not side-products) for each of the following reactions.
cold
DMSO
0=
S:
heat
DMSO
3.) Predict the products (including side-products) of the following reactions.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff46a9339-f731-478c-8ecc-10176ffb98b8%2F0d44b09d-49dd-457f-bac1-f03d3468b09a%2Fdiytf0i_processed.png&w=3840&q=75)
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- 4. Protonation of alcohol A and subsequent loss of water, produces the intermediate B. CH3 CH; CH, CH, — с — сH, CH, CH;CH, - C- CH, CH; | OH A B (a) (i) Name alcohol A. (11) What type of species is intermediate B? (iii) Draw the structures of the two alkenes which can be formed from species B by removal of a proton. Label as C the alkene which shows geometrical isomerism. (b) The intermediate B is readily attacked by nucleophiles such as water. What is the essential feature of a nucleophile? (c) State what final colour you would see if alcohol A were warmed with acidified potassium dichromate(VI). Explain your answer. Colour Explanation . (ii) Draw two structural isomers of alcohol A which form branched chain ketones when heated with acidified potassium dichromate(VI), but which could not form alkene C on dehydration.5. Using curved arrows show the mechanism for the hydrohalogenation for the following reaction. Show how the two possible intermediate products are formed and explain why only one product proceeds to form the product. Clearly indicate attack of electrons and full and partial (8) charges. H-Br Br H-Br Product Intermediate ProductsHi! I need the part b and part c (the products and then the names of them). Please explain if possible!!
- Question 58 Complete the statement below by predicting the major product Use the pool of possible compounds provided in the table. Write the letter exactly as it appears in the table Do not s numbers The reaction (k) below leads to the following major product Write the letter in UPPERCASE corresponding to the structure (in the table provided) that is the best possible match for the pre product. (k) KMnO, OH (warm, concd.) Firacemic TABLE OF POSSIBLE PRODUCTSa) Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium azide by adding curved arrows. b) Complete the product structure by adding any missing atoms, bonds, charges, and nonbonding electrons. Omit curved arrows. :CI: Na ci: Na EN EN N= EN J. 1) LAH 2) H20 c) Predict the organic product of the LAH reduction and hydrolysis steps; include nonbonding electrons. Do not include any inorganic products.Draw the major projects for both organic reactions
- Draw the product(s) of the following reactions. H2 Lindlar catalyst H3C- CEC-CH, Consider E/Z stereochemistry of alkenes. If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down me Separate multiple products using the + sign from the drop-down menu. ору Bste ChemDoodle Submit Answer Retry Entire Group No more group attempts remainWould the change in free energy for each be correct? I'm also confused on C3. Draw the reaction mechanism for the following reactions. When possible, label nucleophiles/electrophiles, carbocations, and oxonium ions. H* CI. a) H. + H2O + НОCHЗ H* OH H* H;C
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