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How would you synthesize the following products? Thank
you!
Y 3. How would you synthesize the...
how to synthesize the following compunds following compands How to synthesize the CHACHz 1. CH 3...
how to synthesize the following compunds
following compands How to synthesize the CHACHz 1. CH 3 BO -(CH2)₂ CH₃ 4 6000 Phone 4. CH₃ CH₂ Br - CH3CH2CH₂CH2Br
Starting with benzene, how would you synthesize the following products? You can use any chemical you...
Starting with benzene, how would you synthesize the following
products? You can use any chemical you can find from chapter 7- 13,
or 16-18 to help you in your synthesis. (15 pts, 5 points
each)
3. Starting with benzene, how would you synthesize the following products? You can use any chemical you can find from chapter 7-13, or 16-18 to help you in your synthesis. (15 pts, 5 points each) OH o-bo
11. How would you synthesize the following compound starting with optically pure (R)-2-butanol (note: it could...
11. How would you synthesize the following compound starting with optically pure (R)-2-butanol (note: it could require multiple steps)? HCN HC CH 12. Give the product of the following reaction: СНЫBr NASH Page 2
Problem #3 Show how you would synthesize the compound represented in the Fischer projection below starting...
Problem #3 Show how you would synthesize the compound represented in the Fischer projection below starting from acetylene. You may use any other reagent necessary. HC-OH HC-OH Extra Credit When treated with hydrogen and a platinum catalyst, an unknown compound X absorbs 5 equivalents of hydrogen to give 7-butylcyclohexane. Treatment of X with an excess of ozone, followed by dimethyl sulfide and water, gives the products shown below. Propose a structure for X.
How would you synthesize the following reactions? a. H3C CH3 b. Br H3C CH3 Br
How would you synthesize the following reactions? a. H3C CH3 b. Br H3C CH3 Br
sbow how you woukd synthesize each of the following compounds from benzene (a) Show how you...
sbow how you woukd synthesize each of the following compounds from
benzene
(a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
10% how how you would synthesize the following compound starting with bromocyclopentane Provide the structure of...
10% how how you would synthesize the following compound starting with bromocyclopentane Provide the structure of the intermediates after each step series. Br Multiple Steps он он
skip 5b 4. Show how you would synthesize the following aldehydes by adding the appropriate Grignard reagent to f...
skip 5b
4. Show how you would synthesize the following aldehydes by adding the appropriate Grignard reagent to formaldehyde. (a) H (b) H 5. Predict the products of the following reactions: (a) 1.) LIAIH 2.) H,0 (b) CH,CH2CH2CH,CENH CH,CH,M B , then H,0* + 1.) DIBAL-H (-78 C) (c) 2.) H,O OCH3 1) DIBAL-H (-78 C) 2.) H,O 3
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds...
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
Show how you would synthesize the following compound starting with acetylene and compounds containing no more...
Show how you would synthesize the following compound starting
with acetylene and compounds containing no more than two carbon
atoms as organic starting material. You may use any additional
reagents you need
Br H H Br
how to synthesize the following compunds
following compands How to synthesize the CHACHz 1. CH 3 BO -(CH2)₂ CH₃ 4 6000 Phone 4. CH₃ CH₂ Br - CH3CH2CH₂CH2Br
Starting with benzene, how would you synthesize the following
products? You can use any chemical you can find from chapter 7- 13,
or 16-18 to help you in your synthesis. (15 pts, 5 points
each)
3. Starting with benzene, how would you synthesize the following products? You can use any chemical you can find from chapter 7-13, or 16-18 to help you in your synthesis. (15 pts, 5 points each) OH o-bo
11. How would you synthesize the following compound starting with optically pure (R)-2-butanol (note: it could require multiple steps)? HCN HC CH 12. Give the product of the following reaction: СНЫBr NASH Page 2
Problem #3 Show how you would synthesize the compound represented in the Fischer projection below starting from acetylene. You may use any other reagent necessary. HC-OH HC-OH Extra Credit When treated with hydrogen and a platinum catalyst, an unknown compound X absorbs 5 equivalents of hydrogen to give 7-butylcyclohexane. Treatment of X with an excess of ozone, followed by dimethyl sulfide and water, gives the products shown below. Propose a structure for X.
How would you synthesize the following reactions? a. H3C CH3 b. Br H3C CH3 Br
sbow how you woukd synthesize each of the following compounds from
benzene
(a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
10% how how you would synthesize the following compound starting with bromocyclopentane Provide the structure of the intermediates after each step series. Br Multiple Steps он он
skip 5b
4. Show how you would synthesize the following aldehydes by adding the appropriate Grignard reagent to formaldehyde. (a) H (b) H 5. Predict the products of the following reactions: (a) 1.) LIAIH 2.) H,0 (b) CH,CH2CH2CH,CENH CH,CH,M B , then H,0* + 1.) DIBAL-H (-78 C) (c) 2.) H,O OCH3 1) DIBAL-H (-78 C) 2.) H,O 3
7. Synthesis Problem (15 points) Show how you would synthesize 3 of the 4 following compounds in one chemical reaction. You may use any starting material you wish and any organic and inorganic reagents. Clearly indicate which ones you want graded by circling the molecules н, осн, Br ОН
Show how you would synthesize the following compound starting
with acetylene and compounds containing no more than two carbon
atoms as organic starting material. You may use any additional
reagents you need
Br H H Br
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