Predict the major organic product(s) for each of the following reactions. Be sure to show stereochemistry when appropriate. 1) OsO4/THF 2) H₂S
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Q: 9.1 Name the compound shown below.
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- 1) Redraw the structure and assign E or Z configuration to each double bond in the molecule. 2) Draw the organic products obtained from the ozonolysis of the compound, using a reductive work-up with zinc/HAc.Illustrated below is the hydrolysis of a C-C bond (in the first molecule) hydrolyzed by water (2nd molecule). Which pair of open boxes best identifies the location of the (-H) and (-OH) components of water on the products. Choose one from the following: (a) A (b) B (c) C (d) DPredict the major organic product of each reaction or provide the reagents needed to complete each transformation.
- Which one of the statements below is wrong about Zaitsev’s Rule. a. None of the above b. The Zaitsev’s Rule demonstrate the principle of regioselectivity in elimination reactions c. The more substituted alkene is the major product of E1 or E2 elimination d. The more substituted alkane product is obtained when a proton is removed from β-carbon that is bonded to the fewest hydrogens e. The most stable alkene is generally the major productShow how to prepare each alkyne from the given starting material. In part (c), D indicates deuterium. Deuterium-containing reagents such as BD3, D2O, and CH3COOD are available commercially.Indicate how to synthesize the following compounds in two or more stages by showing all required reagents (organic and inorganic). DO NOT SHOW THE MECHANISM. This is an organic chemistry exercise.
- Give reasons for the following :(i) Ethyl iodide undergoes SN2 reaction faster than ethyl bromide.(ii) (±) 2-Butanol is optically inactive.(iii) C—X bond length in halobenzene is smaller than C—X bond length in CH3—X.When 1,2-cyclohexanediol is dehydrated in the presence of concentrated sulfuric acid, the major product is not an alkene. Instead, you get cyclohexanone. Write a reasonable and detailed mechanism for the dehydration of 1,2-cyclohexanediol to form cyclohexanone. Use curved arrows to show the flow of electrons and draw the structures of all intermediates and byproducts formed in the course of this reaction as well as any alternative resonance structures that will help you to account for the formation of the major product observed in this reaction.What is going on from compound B to compound C? Can you please select all the options that apply
- The bicyclo [3.1.0] hexane ring system, highlighted in compound 3, is found in several natural products, including sabinene, a compound partially responsible for the flavor of ground black pepper. One method for preparing this ring system involves the conversion of compound 1 to compound 2, as shown below. Draw the structure of compound 2 and provide a reasonable mechanism for its formation. Add any remaining curved arrows to complete step one of the mechanism, and modify the given drawing as needed to show the intermediate that is formed in this step.Please give a step by step for this problem. Give the major organic products.NaNH2 is typically used instead of KOH to produce alkynes through elimination because NaNH2 is a stronger base. Explain why KOH can be used to create diphenylacetylene.