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The flow chart below shows the importance of ethylene oxide in organic synthesis. a) Provide the...
use DETAILED explanations and reagents that are commonly used in organic chemistry to prove this synthesis....
use DETAILED explanations and reagents that are commonly used in
organic chemistry to prove this synthesis. DO NOT FORGET to show
movement of electrons, and explain why you used each reagent.
Propose the synthesis for 1,3-cyclohexadiene from cyclohexene. Show the complete mechanism for each step of the reaction and all intermediates formed.
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B...
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 in slope fin Step 2 Hint: you can use Br 1. H', ethylene glycol, heat 2. NaOH/H, O, heat 3. H30* Product A Step 3 HCl dilute Product C Product B 1. PhMgBr, ether 2. H20 acetone Step 1: Step 2: Step 3: 3. Show the full mechanism of Step 3...
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B...
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 Step 2 Hint: can use you 1. H, ethylene glycol, heat 2. NaOHH2o, heat 3. Н,о" Br Product A Step 3 HCI dilute PhMgBr, ether Product C Product B acetone 2. H,о" Step 1: Step 2: Step 3:
What is the structure of the last box? Below is a three-step synthesis. Provide the missing...
What is the structure of the last box?
Below is a three-step synthesis. Provide the missing organic products for each step. Do not add inorganic side-products or minor products. CH3 1. BH3 THF HBr NaOtBu, HOtBu 6th attempt Feedback i See Periodic Table See Hint 9% 0% HBr NaOtBu BH3/H202 он
can someone who is an expert on organic chemistry answer these; this is graded! thank you!...
can someone who is an expert on organic chemistry answer
these; this is graded! thank you!
3. Design concise syntheses for the following transformations. Show all reactants, reagents, and products for each step. a) i ako NH2 INH = 5 to z toho OON 4. Provide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these...
Experiment Questions What is an epoxide and how is it useful with respect to synthesis design?...
Experiment Questions What is an epoxide and how is it useful with respect to synthesis design? • What are typical reagents used for epoxidation? • What is the mechanism for epoxidation? Must stereospecificity be considered? Experiment Techniques • Use of sodium bisulfite wash to remove excess peroxy acid from reaction mixture. Introduction By now you are well aware that the product of previous experiment (reaction of cyclohexanol and acid) is an alkene. You should also be storing key reactions of...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction mechanism. Be sure to include important intermediate compounds, electron flow arrows, and formal charges for full credit. ОН 1. SOCl2, pyridine 2. CH3NH2 (10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with Correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10...
Provide a flow chart detailing the acid/base extraction/separation of the compounds show below. Your answer must...
Provide a flow chart detailing the acid/base extraction/separation of the compounds show below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M), 10% sodium bicarbonate (aq). Clearly indicate the product(s) and layers formed following each step of your separation scheme. IMPORTANT: p-cresol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. 2-ethylbenzoic acid is soluble in both sodium hydroxide and sodium bicarbonate solutions. Use...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyri...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below. Your answer must...
Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid M 6M), sodium hydroxide (IM & 6M),10% sodium bicarbonate (aq Clearly indicate the product(s) and layers formedfollowing each step of your separation scheme. HINT: phenol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. Benzoic acid is soluble in both sodium hydroxide and sodium bicarbonate solutions. Use skeletal structures only...
use DETAILED explanations and reagents that are commonly used in
organic chemistry to prove this synthesis. DO NOT FORGET to show
movement of electrons, and explain why you used each reagent.
Propose the synthesis for 1,3-cyclohexadiene from cyclohexene. Show the complete mechanism for each step of the reaction and all intermediates formed.
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 in slope fin Step 2 Hint: you can use Br 1. H', ethylene glycol, heat 2. NaOH/H, O, heat 3. H30* Product A Step 3 HCl dilute Product C Product B 1. PhMgBr, ether 2. H20 acetone Step 1: Step 2: Step 3: 3. Show the full mechanism of Step 3...
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 Step 2 Hint: can use you 1. H, ethylene glycol, heat 2. NaOHH2o, heat 3. Н,о" Br Product A Step 3 HCI dilute PhMgBr, ether Product C Product B acetone 2. H,о" Step 1: Step 2: Step 3:
What is the structure of the last box?
Below is a three-step synthesis. Provide the missing organic products for each step. Do not add inorganic side-products or minor products. CH3 1. BH3 THF HBr NaOtBu, HOtBu 6th attempt Feedback i See Periodic Table See Hint 9% 0% HBr NaOtBu BH3/H202 он
can someone who is an expert on organic chemistry answer
these; this is graded! thank you!
3. Design concise syntheses for the following transformations. Show all reactants, reagents, and products for each step. a) i ako NH2 INH = 5 to z toho OON 4. Provide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these...
Experiment Questions What is an epoxide and how is it useful with respect to synthesis design? • What are typical reagents used for epoxidation? • What is the mechanism for epoxidation? Must stereospecificity be considered? Experiment Techniques • Use of sodium bisulfite wash to remove excess peroxy acid from reaction mixture. Introduction By now you are well aware that the product of previous experiment (reaction of cyclohexanol and acid) is an alkene. You should also be storing key reactions of...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction mechanism. Be sure to include important intermediate compounds, electron flow arrows, and formal charges for full credit. ОН 1. SOCl2, pyridine 2. CH3NH2 (10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with Correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10...
Provide a flow chart detailing the acid/base extraction/separation of the compounds show below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M), 10% sodium bicarbonate (aq). Clearly indicate the product(s) and layers formed following each step of your separation scheme. IMPORTANT: p-cresol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. 2-ethylbenzoic acid is soluble in both sodium hydroxide and sodium bicarbonate solutions. Use...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid M 6M), sodium hydroxide (IM & 6M),10% sodium bicarbonate (aq Clearly indicate the product(s) and layers formedfollowing each step of your separation scheme. HINT: phenol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. Benzoic acid is soluble in both sodium hydroxide and sodium bicarbonate solutions. Use skeletal structures only...
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