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Question 5. (16 marks) Complete the reactions to show the multi-step syntheses of each product. Reaction conditions go...
3) Complete the reactions to show the multi-step syntheses of each product from (R)-2 bromo-3-methylbutane. Reaction...
3) Complete the reactions to show the multi-step syntheses of each product from (R)-2 bromo-3-methylbutane. Reaction conditions go in boxes above arrows (1 reaction/box) Complete the template molecules provided to show each step of the synthesis. [20] Hint- This question involves addition, elimination, substitution and alcohol chemistry Br (R)-2-bromo-3-methylbutane 3-methylbutan-1-ol (R)-2-bromo-3-methylbutane (R)-3-bromo-2 methylbutan-2-ol (R)-2-bromo-3-methylbutane (1-chloro-2-methylbutane (R)-2-bromo-3-methylbutane CN ()-1-cyano-3-methylbutan-1-ol
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each...
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
14-15) Predict the product. Show each step. 16-17) Predict the product. If no reaction, write NR....
14-15) Predict the product. Show each step.
16-17) Predict the product. If no reaction, write NR.
14.) Predict the product. Show each step. of CH₂Br 2) con 7.) Mg 3.) H₂or 15.) Predict the product, Show each step 1.) Soch 2.) Li Al(O+-BuzH 16.) Predict the products. If no reaction, write NR. of ccl + CH₃OH Ht 1.) @ My Br Excess 2.) H₃O+ 7
Please show each step What is the expected major product for the following reaction? 1. Hg(ОАс)2,...
Please show each step
What is the expected major product for the following reaction? 1. Hg(ОАс)2, НО 2. NaBH4, NaOH ОН * ОН + enantiomer + enantiomer + enantiomer + enantiomer + enantiomer Ооооо
show the mechansim pf each step in each question Give the product for the following reaction....
show the mechansim pf each step in each question
Give the product for the following reaction. CH:CH -CH:CHCH: 1. NaBH, > 2. H.O . Give the product for the following reaction. CH, CH H 1 CHỊ H. H 2. HO 3. NaBH(O,CCH) Give the product for the following reaction. 1. (CH, H, H CH: 2. H0 3. NaHCO.CCHE, Give the product for the following reaction. 1. H.NOH, H CH:CH- СН: 2.-H.0 3. HPC
please show each step. Question 5 What is the major organic product of the following sequence...
please show each step.
Question 5 What is the major organic product of the following sequence of reactions? Type is systematic IUPAC rame in the box below 1) Bry, hy 2) Mg, ether 3) CO2 Isobutane 4) H30* 5) SOCH 6) excess NH) Selected Answer 2.2 dimethylpropanamide
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in...
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in methanol (Na* OCH, CH,OH). CH NaOme MeOH CH Compound A Problem 2c Draw the major expected organic product (a) Redraw Compound A as seen in Viewpoint I below left as a Newman projection on the template provided in Problem 2a (below). Hint: Fill in missing Hs ar C2 and C3 to help you get started! (b) Rotate the C2 C3 bond to obtain the...
3) Complete the reactions to show the multi-step syntheses of each product from (R)-2 bromo-3-methylbutane. Reaction conditions go in boxes above arrows (1 reaction/box) Complete the template molecules provided to show each step of the synthesis. [20] Hint- This question involves addition, elimination, substitution and alcohol chemistry Br (R)-2-bromo-3-methylbutane 3-methylbutan-1-ol (R)-2-bromo-3-methylbutane (R)-3-bromo-2 methylbutan-2-ol (R)-2-bromo-3-methylbutane (1-chloro-2-methylbutane (R)-2-bromo-3-methylbutane CN ()-1-cyano-3-methylbutan-1-ol
2. Design multi-step syntheses for TWO of the following targets. Show the reagents needed for each step and the product of each step. Special conditions: You must use cyclopentadiene as your starting material for all syntheses. You may use organic reagents containing 4 or fewer carbons, and any inorganic reagents. For any Diels-Alder reaction that you use (necessary for all targets!), the dienophile must be an a,ß-unsaturated carbonyl compound. Target 1: HO D Target 2: Doe Target 3: ro Target...
14-15) Predict the product. Show each step.
16-17) Predict the product. If no reaction, write NR.
14.) Predict the product. Show each step. of CH₂Br 2) con 7.) Mg 3.) H₂or 15.) Predict the product, Show each step 1.) Soch 2.) Li Al(O+-BuzH 16.) Predict the products. If no reaction, write NR. of ccl + CH₃OH Ht 1.) @ My Br Excess 2.) H₃O+ 7
Please show each step
What is the expected major product for the following reaction? 1. Hg(ОАс)2, НО 2. NaBH4, NaOH ОН * ОН + enantiomer + enantiomer + enantiomer + enantiomer + enantiomer Ооооо
show the mechansim pf each step in each question
Give the product for the following reaction. CH:CH -CH:CHCH: 1. NaBH, > 2. H.O . Give the product for the following reaction. CH, CH H 1 CHỊ H. H 2. HO 3. NaBH(O,CCH) Give the product for the following reaction. 1. (CH, H, H CH: 2. H0 3. NaHCO.CCHE, Give the product for the following reaction. 1. H.NOH, H CH:CH- СН: 2.-H.0 3. HPC
please show each step.
Question 5 What is the major organic product of the following sequence of reactions? Type is systematic IUPAC rame in the box below 1) Bry, hy 2) Mg, ether 3) CO2 Isobutane 4) H30* 5) SOCH 6) excess NH) Selected Answer 2.2 dimethylpropanamide
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in methanol (Na* OCH, CH,OH). CH NaOme MeOH CH Compound A Problem 2c Draw the major expected organic product (a) Redraw Compound A as seen in Viewpoint I below left as a Newman projection on the template provided in Problem 2a (below). Hint: Fill in missing Hs ar C2 and C3 to help you get started! (b) Rotate the C2 C3 bond to obtain the...
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