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1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions...
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions th...
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit.
1. Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions...
1. Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. (4 pts each) a. H F b. но OH
Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that...
Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of 1. stereochemical details. (4 pts each) a b. но ОН For each reaction below, please draw the starting material or the major (singular) product, including any pertinent stereochemical details. (3 pts each) 2. a. 3. Hg(OAc)2, D20 2. KOt-Bu 1.TsCl Он 4. NaBH t-BuOH EtgN etherol b. 3. СHBES 2. LDA 1. HBr KOt-Bu,...
2. Provide conditions for the following reactions mations for the following reactions. More than one step...
2. Provide conditions for the following reactions mations for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and stereochemical details. Additionally, if the product(s) listed would exhibit op circle it/them. (14 pts) at would give you the optimum yield, and be mindful of ally, if the product(s) listed would exhibit optical activity, HO + enantiomer in the bord for the com HO
31) Provide the reagents necessary to complete the following transformation. More than one step is needed....
31) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. CH он 32) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. Br он enantiomer HO tto prss 33) Provide the reagents necessary to convert 3-methyl-2-butanol into 2-methyl-2-butanol. More than step is needed. Show the structures of any intermediate products. Page 7 of 8
1. Provide the necessary reaction conditions (reagents and solvents) to perform the indicated transformation. More than...
1. Provide the necessary reaction conditions (reagents
and solvents) to perform the indicated transformation. More than
one step may be necessary. Synthesis of reagents used in the
transformation are not required. Consider equivalents, selectivity,
and stereochemistry. Very little partial credit will be
given.
مل مل . . است Me OH CH سرعت -- له Me Me OH Me H0 Me Me- DH - We Me لكم OH 0 م --کمت و سلم . یک ما لكم . Me Me Me
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may...
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may be needed. Show all reagents and synthetic intermediates.
Each of the following syntheses may require more than one step. Provide the reagents and intermediates...
Each of the following syntheses may require more than one step.
Provide the reagents and intermediates for each step from the
starting reagent to the final product.
H H and prepare CH3CH-CH2 (a) Start with CH3 CH3 and prepare (b) Start with OC(CH3)3 and prepare and any 2 carbon fragment (c) Start with CH3CH CH2 СH, and prepare (d) Start with
Provide the missing reagents for the following reactions. (Hint: There may be more than 1 step)...
Provide the missing reagents for the following reactions. (Hint: There may be more than 1 step) (4pts each) OH НО. Continued on next page. Draw a plausible stepwise mechanism for the following transformation. Include all steps of the reaction. (5pts) Bry, hy Br
Provide the missing reagents for the following reactions. (Hint: There may be more than 1 step)...
Provide the missing reagents for the following reactions. (Hint: There may be more than 1 step) (4pts each) OH НО. Continued on next page. Draw a plausible stepwise mechanism for the following transformation. Include all steps of the reaction. (5pts) Bry, hy Br
1. Provide conditions for the following transformation. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. No mechanisms are needed. You may want to show intermediates to better help with your thought process and partial credit.
1. Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of stereochemical details. (4 pts each) a. H F b. но OH
Provide conditions for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and be mindful of 1. stereochemical details. (4 pts each) a b. но ОН For each reaction below, please draw the starting material or the major (singular) product, including any pertinent stereochemical details. (3 pts each) 2. a. 3. Hg(OAc)2, D20 2. KOt-Bu 1.TsCl Он 4. NaBH t-BuOH EtgN etherol b. 3. СHBES 2. LDA 1. HBr KOt-Bu,...
2. Provide conditions for the following reactions mations for the following reactions. More than one step may be needed. Incorporate conditions that would give you the optimum yield, and stereochemical details. Additionally, if the product(s) listed would exhibit op circle it/them. (14 pts) at would give you the optimum yield, and be mindful of ally, if the product(s) listed would exhibit optical activity, HO + enantiomer in the bord for the com HO
31) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. CH он 32) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. Br он enantiomer HO tto prss 33) Provide the reagents necessary to convert 3-methyl-2-butanol into 2-methyl-2-butanol. More than step is needed. Show the structures of any intermediate products. Page 7 of 8
1. Provide the necessary reaction conditions (reagents
and solvents) to perform the indicated transformation. More than
one step may be necessary. Synthesis of reagents used in the
transformation are not required. Consider equivalents, selectivity,
and stereochemistry. Very little partial credit will be
given.
مل مل . . است Me OH CH سرعت -- له Me Me OH Me H0 Me Me- DH - We Me لكم OH 0 م --کمت و سلم . یک ما لكم . Me Me Me
2. (4 pts.) Provide a reasonable synthesis for the following transformations. More than one step may be needed. Show all reagents and synthetic intermediates.
Each of the following syntheses may require more than one step.
Provide the reagents and intermediates for each step from the
starting reagent to the final product.
H H and prepare CH3CH-CH2 (a) Start with CH3 CH3 and prepare (b) Start with OC(CH3)3 and prepare and any 2 carbon fragment (c) Start with CH3CH CH2 СH, and prepare (d) Start with
Provide the missing reagents for the following reactions. (Hint: There may be more than 1 step) (4pts each) OH НО. Continued on next page. Draw a plausible stepwise mechanism for the following transformation. Include all steps of the reaction. (5pts) Bry, hy Br
Provide the missing reagents for the following reactions. (Hint: There may be more than 1 step) (4pts each) OH НО. Continued on next page. Draw a plausible stepwise mechanism for the following transformation. Include all steps of the reaction. (5pts) Bry, hy Br
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