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1. Give the IUPAC name for each of the following structures. Include stereochemistry when appropriate. non...
Name 1. Give a correct name for each of the following compounds. Include stereochemistry when appropriate....
Name 1. Give a correct name for each of the following compounds. Include stereochemistry when appropriate. CH3 H -OH -Br H- Br CH2CH3 HO OH 2. Draw the following compounds १०ofion) lii
Predict the major products of the following reactions, and give the structures of any intermediates. Include...
Predict the major products of the following reactions,
and give the structures of any intermediates. Include
stereochemistry where appropriate
.
s-46 Predict the major predueowing reactions, and give the structures of any intermediates. Include stereochemistry where appropriate (l BH, THF (2) H,O, OH CCl, () 0, (-78 C) (2) (CH31,5 へ HCI ROOR KMno OH CH,CO,H H. H,0 KMnO, OH (warm, coned.) ) (l)03 (-78 °C) (2) (CH,S ·H20 MI- CHR Pt (0) Cl2 H,0 (2) NaBH 7 Limonene is...
1. give an appropriate systematic (IUPAC) name for each of the following compounds. 2. for each...
1.
give an appropriate systematic (IUPAC) name for each of the
following compounds.
2. for each of the following reactions involving carboxylic
acid derivatives, give the expected product. If no reaction is
expected, write "no reaction". You may assume that any needed
acid/base catalysts are present.
ive an appropriate systematic (IUPAC) name for each of the following compounds. Hold 2. For each of the following reactions involving carboxylic acid derivatives, give the expected product. If no reaction is expected, write...
Fill in the boxes with the appropriate structures and reagents. Include stereochemistry. Please helpppppp Please fill...
Fill in the boxes with the appropriate structures and
reagents. Include stereochemistry. Please helpppppp
Please fill in the boxes with the appropriate structures and reagents. Include stereochemistry where necessary and do not use reagent abbreviations. (4 points each) OEt он SOCI2 Me2Culi NC OH KCN HCN HCI H2O HONH2
(References) Not Submitted Give IUPAC names for the following structures. If appropriate, specify relative stereochemistry. 1st...
(References) Not Submitted Give IUPAC names for the following structures. If appropriate, specify relative stereochemistry. 1st structure: 1,3- 2nd structure: cyclopropoxy Submit Answer Try Another Version 10 item attempts remaining Br + HCECH + H2C-CH, H₂C & ОН Hic . Hoc m -CECH Br HCECH OTBDMS OTBDMS H3C OTBDMS HC OH HEC Shown above is the stepwise synthesis of (7Z, TIE)-7,11-hexadecadien-1-ol, the key intermediate for synthesis of Gossyplure, the sex pheromone of the pink bollworm. From the choices provided below,...
Give the IUPAC name, including the R or S designations when appropriate, of each of the...
Give the IUPAC name, including the R or S designations when appropriate, of each of the following compounds. CHз НОМ СН2СІ н СН3 d) H- Hзс OH -ОН
give the appropriate IUPAC name for the following structure formula of a halogenated compound Give the appropriate...
give the appropriate IUPAC name for the following structure
formula of a halogenated compound
Give the appropriate IUPAC name for the following structural formula of a halogenated compound. Br, CH3 (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis trans writing compound names.) Name: pt pt Submit Answer T ry Another Version 10 item attempts remainin 1 pt 1 pt 1 pt 1 pt 1 pt 1 pr 1 pt
Give the IUPAC name for the following structures: Part II: Give the IUPAC name for each...
Give the IUPAC name for the following structures:
Part II: Give the IUPAC name for each of the following structures. (10 marks) 1. нс. CH CH3 CH3 2. нс. CH3 CH3 CH3 3 -CH3 CH3 CH3 4. F CH3 CI 5. À 6. HC CH3 Br CH3 H 7. H 8. H3C 9. HC CI HC CHE 10. H3c CH3
Rere Give the IUPAC name for the following structure. If appropriate, specify stereochemistry. Ph-S-NH2 O=O=O IUPAC...
Rere Give the IUPAC name for the following structure. If appropriate, specify stereochemistry. Ph-S-NH2 O=O=O IUPAC name: Submit Answer Try Another Version 5 item attempts remair
Give the IUPAC name for each of the following compounds. Use R/S or cis/trans when appropriate...
Give the IUPAC name for each of the following compounds. Use R/S
or cis/trans when appropriate
Q1.4 4 Points НСО Enter your answer here Q1.5 4 Points OH ko Enter your answer here
Name 1. Give a correct name for each of the following compounds. Include stereochemistry when appropriate. CH3 H -OH -Br H- Br CH2CH3 HO OH 2. Draw the following compounds १०ofion) lii
Predict the major products of the following reactions,
and give the structures of any intermediates. Include
stereochemistry where appropriate
.
s-46 Predict the major predueowing reactions, and give the structures of any intermediates. Include stereochemistry where appropriate (l BH, THF (2) H,O, OH CCl, () 0, (-78 C) (2) (CH31,5 へ HCI ROOR KMno OH CH,CO,H H. H,0 KMnO, OH (warm, coned.) ) (l)03 (-78 °C) (2) (CH,S ·H20 MI- CHR Pt (0) Cl2 H,0 (2) NaBH 7 Limonene is...
1.
give an appropriate systematic (IUPAC) name for each of the
following compounds.
2. for each of the following reactions involving carboxylic
acid derivatives, give the expected product. If no reaction is
expected, write "no reaction". You may assume that any needed
acid/base catalysts are present.
ive an appropriate systematic (IUPAC) name for each of the following compounds. Hold 2. For each of the following reactions involving carboxylic acid derivatives, give the expected product. If no reaction is expected, write...
Fill in the boxes with the appropriate structures and
reagents. Include stereochemistry. Please helpppppp
Please fill in the boxes with the appropriate structures and reagents. Include stereochemistry where necessary and do not use reagent abbreviations. (4 points each) OEt он SOCI2 Me2Culi NC OH KCN HCN HCI H2O HONH2
(References) Not Submitted Give IUPAC names for the following structures. If appropriate, specify relative stereochemistry. 1st structure: 1,3- 2nd structure: cyclopropoxy Submit Answer Try Another Version 10 item attempts remaining Br + HCECH + H2C-CH, H₂C & ОН Hic . Hoc m -CECH Br HCECH OTBDMS OTBDMS H3C OTBDMS HC OH HEC Shown above is the stepwise synthesis of (7Z, TIE)-7,11-hexadecadien-1-ol, the key intermediate for synthesis of Gossyplure, the sex pheromone of the pink bollworm. From the choices provided below,...
Give the IUPAC name, including the R or S designations when appropriate, of each of the following compounds. CHз НОМ СН2СІ н СН3 d) H- Hзс OH -ОН
give the appropriate IUPAC name for the following structure
formula of a halogenated compound
Give the appropriate IUPAC name for the following structural formula of a halogenated compound. Br, CH3 (Where stereochemistry is shown, include a designation of configuration in your answer. Use cis trans writing compound names.) Name: pt pt Submit Answer T ry Another Version 10 item attempts remainin 1 pt 1 pt 1 pt 1 pt 1 pt 1 pr 1 pt
Give the IUPAC name for the following structures:
Part II: Give the IUPAC name for each of the following structures. (10 marks) 1. нс. CH CH3 CH3 2. нс. CH3 CH3 CH3 3 -CH3 CH3 CH3 4. F CH3 CI 5. À 6. HC CH3 Br CH3 H 7. H 8. H3C 9. HC CI HC CHE 10. H3c CH3
Rere Give the IUPAC name for the following structure. If appropriate, specify stereochemistry. Ph-S-NH2 O=O=O IUPAC name: Submit Answer Try Another Version 5 item attempts remair
Give the IUPAC name for each of the following compounds. Use R/S
or cis/trans when appropriate
Q1.4 4 Points НСО Enter your answer here Q1.5 4 Points OH ko Enter your answer here
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