Synthesize the following compound from cyclohexanone and organic halides having ≤ 4 C's. You may use any other inorganic reagents.
Draw all reaction intermediates, and select the single best set of reagents for each of the four reaction steps. Cyclohexanone
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Synthesize the following compound from cyclohexanone and organic halides having ≤ 4 C's
Be sure to answer all parts. Convert acetophenone (CoHl,COCH,) into the following compound. You may use...
Convert acetophenone (C6H5COCH3) into the following compound. You may use any other organic compounds or required inorganic reagents. Draw both reaction intermediates, and select the single best set of reagents for each of the three reactio steps.
6. (12 points) Synthesize the following compound from acetophenone. Use may use any available organic and...
6. (12 points) Synthesize the following compound from acetophenone. Use may use any available organic and inorganic reagents: from
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and...
Synthesize this from 4 carbon or less alcohols and any organic
or inorganic reagents needed and any inorganic compounds. Include
all mechanisms, steps, reagents, and reactions used.
СН3 NH2 СН3
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and...
Synthesize this from 4 carbon or less alcohols and any organic
or inorganic reagents needed and any inorganic compounds.
Include all mechanisms, steps, reagents, and reactions used.
CH3 NH2 СН3
extra credit orgo chem NaBH MOH 1.Write two starting materials (five or fewer C's) that react...
extra credit orgo chem
NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
Synthesis 18.63) Synthesize each compound from benzene and any other organic or inorganic reagents. Br- CICINO,...
Synthesis 18.63) Synthesize each compound from benzene and any other organic or inorganic reagents. Br- CICINO, OYNH2 COOH O2N. -C NH2 НО ОН SO3H HOOC (PABA) sunscreen component
_________________________________________________________________________________________________________________________________ d. Prepare octane from 1-pentyne, indicate each needed reagents. e. Synthesize cis-2-hexene from 1-pentyne and...
_________________________________________________________________________________________________________________________________
d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
Provide a synthetic route for the following compound from benzene and any other necessary organic and...
Provide a synthetic route for the following compound from
benzene and any other necessary organic and inorganic reagents.
List the required reagents and conditions for each step and draw
the product for each step
14. Provide a synthetic route for the following compound from benzene and any other necessary organic and inorganic reagents. List the required reagents and conditions for each step and draw the product for each step. (4 pts) 0-V
8. Predict the number of peaks and the 'H splitting (multiplicity) for the following compound: он...
8. Predict the number of peaks and the 'H splitting (multiplicity) for the following compound: он Outline the synthetic steps necessary to synthesize the compound below. You may use any organic or inorganic reagents you need but no more than 3 carbons starting compounds. Show the structures of all intermediate compounds that would probably be isolated during the course of your synthesis, and show all necessary reagents 9.
Synthesis with 10 steps or less Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) ca...
Synthesis with 10 steps or less
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
6. (12 points) Synthesize the following compound from acetophenone. Use may use any available organic and inorganic reagents: from
Synthesize this from 4 carbon or less alcohols and any organic
or inorganic reagents needed and any inorganic compounds. Include
all mechanisms, steps, reagents, and reactions used.
СН3 NH2 СН3
Synthesize this from 4 carbon or less alcohols and any organic
or inorganic reagents needed and any inorganic compounds.
Include all mechanisms, steps, reagents, and reactions used.
CH3 NH2 СН3
extra credit orgo chem
NaBH MOH 1.Write two starting materials (five or fewer C's) that react to form the target molecule starting from any carbonyl compound and any organometallic reagent. OH Part IV. Mechanistic Puzzlers (16 pts) 10. Reduction of cyclohexanone using lithium aluminum hydride gives a deuterated alcohol when D.O is used instead of H.O in the workup step. Account for this outcome with a mechanism, showing curved arrows, the key intermediate, and lone pairs and charges. (6 pts)...
Synthesis 18.63) Synthesize each compound from benzene and any other organic or inorganic reagents. Br- CICINO, OYNH2 COOH O2N. -C NH2 НО ОН SO3H HOOC (PABA) sunscreen component
_________________________________________________________________________________________________________________________________
d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
Provide a synthetic route for the following compound from
benzene and any other necessary organic and inorganic reagents.
List the required reagents and conditions for each step and draw
the product for each step
14. Provide a synthetic route for the following compound from benzene and any other necessary organic and inorganic reagents. List the required reagents and conditions for each step and draw the product for each step. (4 pts) 0-V
8. Predict the number of peaks and the 'H splitting (multiplicity) for the following compound: он Outline the synthetic steps necessary to synthesize the compound below. You may use any organic or inorganic reagents you need but no more than 3 carbons starting compounds. Show the structures of all intermediate compounds that would probably be isolated during the course of your synthesis, and show all necessary reagents 9.
Synthesis with 10 steps or less
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six (6) carbons or less, plus any other organic or inorganic reagents necessary. Determine the IUPAC systematic chemical name for your target compound. Try for io sieps or tesvs
Synthesis Problem Show all the steps required, including intermediates, for the synthesis of the following target compound, using any starting material with six...
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