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3 In the space below, provide the correct IUPAC name for the following structure wa HOW...
Palagraph Name Group What is the IUPAC name for the following compound? OH What is the...
Palagraph Name Group What is the IUPAC name for the following compound? OH What is the IUPAC name for the following compound? COH What is the IUPAC name for the following compound? 4. Provide the structure for 5-chloro-3-oxo-octanoic acid 5. Rank the following acids in decreasing (strongest to weakest) order of acidity.
What is the IUPAC name for the following molecule? OH 6 Η (10 pts) Rank the...
What is the IUPAC name for the following molecule? OH 6 Η (10 pts) Rank the following carbocations in order of most stable to least stable. Explain your ranking. What factors are involved (think about factors for acid strength)?
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral...
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral (meso) compounds below. (4 points) OH COH HOZC OH c. Draw the structure of the compound based on its IUPAC name. (4 points) d. Of the cations below, circle any that are achiral. (4 points) OAC Hg ΤΗ (E)-4-ethyl-3-fluorohept-3-ene e. Provide the IUPAC name of the molecule shown below. (4 points) f Rank the following cations from least stable to most stable. (3 points)...
What is the IUPAC name of the following compound? 4 Rank the following alkenes from most...
What is the IUPAC name of the following compound? 4 Rank the following alkenes from most to least stable. ОН OH ОН IX M A. I > || > III B. I > III > 11 C. II > III > 1 D. III > II > Which carbon would form the most stable carbocation? A D В С Which of the following is a wax at room temperature? A. B. C. D. E. None of these
1. Name the following using IUPAC Naming. ОН HO НО. Name and Rank the following compounds...
1. Name the following using IUPAC Naming. ОН HO НО. Name and Rank the following compounds as Most Acidic, Middle and Least Acid ООН ООН сі
1 Use the structures below to answer the following questions Br Z=0 Br vi 3 1...
1 Use the structures below to answer the following questions Br Z=0 Br vi 3 1 2 a Enter the number of the compound that could undergo Nucleophilic Aromatic Substitution here b Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here c Explain why it will not undergo this reaction in the space below d Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here e Explain...
48. Provide a name for the structure below. (I 4/AC) CH3 L19. Provide a name for...
48. Provide a name for the structure below. (I 4/AC) CH3 L19. Provide a name for the compound below. CAPAC) CH3 CH,CECCHCH2CH2CH3 50. Provide the correct IUPAC name for the following compound. NO2 CH 51. Give an acceptable name for the following substance. IUPAC HOCH,CH OH Name: S7 Provide the IUPAC name for the structure below. H NOZ 53. Provide the IUPAC name for the following structure. OH ОН 54 Draw a structure corresponding to the following IUPAC name. diethyl...
1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3...
1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3 pts.) 2. Draw the bond-line structure of (2,4Z)-2,5-dibromo-3-methylhexa-2,4-diene. (3 pts.) 3. Label the most stable and the least stable alkene (4 pts.) 4. Consider the substitution reaction below. (4 pts.) NaSH DMF SH in why this reaction proceeds through an SN mechanism and not an S2 mechanism a) Explain why this reaction proces o b) Explain why this reaction produces a racemic mixture of...
1. Follow the instructions given: 20 points. a. Provide the IUPAC name for the molecule shown...
1. Follow the instructions given: 20 points. a. Provide the IUPAC name for the molecule shown below. (4 points) b. Provide the IUPAC name for the molecule shown below. (4 points) c. Of the cations shown below, circle any that are chiral. (4 points) d. Draw the expected product of the reaction below and briefly explain why three, not two equivalents of NaNH2 are required. (5 points) Br- 3 NaNH2 NH e. Rank the following radicals in terms of their...
Compound A Compound B Give the IUPAC name for Compound A. 2. Give the IUPAC name...
Compound A Compound B Give the IUPAC name for Compound A. 2. Give the IUPAC name for Compound B. 3. Which compound from above (Compound A or Compound B) is more soluble in water and why? 4. Which compound can be dehydrated to form a double bond (Compound A or Compound B)? Draw the most likely product of that dehydration. (Insert a picture of your drawing of the molecule or a scan of your drawing of the molecule) 5. Could...
Palagraph Name Group What is the IUPAC name for the following compound? OH What is the IUPAC name for the following compound? COH What is the IUPAC name for the following compound? 4. Provide the structure for 5-chloro-3-oxo-octanoic acid 5. Rank the following acids in decreasing (strongest to weakest) order of acidity.
What is the IUPAC name for the following molecule? OH 6 Η (10 pts) Rank the following carbocations in order of most stable to least stable. Explain your ranking. What factors are involved (think about factors for acid strength)?
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral (meso) compounds below. (4 points) OH COH HOZC OH c. Draw the structure of the compound based on its IUPAC name. (4 points) d. Of the cations below, circle any that are achiral. (4 points) OAC Hg ΤΗ (E)-4-ethyl-3-fluorohept-3-ene e. Provide the IUPAC name of the molecule shown below. (4 points) f Rank the following cations from least stable to most stable. (3 points)...
What is the IUPAC name of the following compound? 4 Rank the following alkenes from most to least stable. ОН OH ОН IX M A. I > || > III B. I > III > 11 C. II > III > 1 D. III > II > Which carbon would form the most stable carbocation? A D В С Which of the following is a wax at room temperature? A. B. C. D. E. None of these
1. Name the following using IUPAC Naming. ОН HO НО. Name and Rank the following compounds as Most Acidic, Middle and Least Acid ООН ООН сі
1 Use the structures below to answer the following questions Br Z=0 Br vi 3 1 2 a Enter the number of the compound that could undergo Nucleophilic Aromatic Substitution here b Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here c Explain why it will not undergo this reaction in the space below d Enter the number of one of the compounds that will not undergo Nucleophilic Aromatic Substitution here e Explain...
48. Provide a name for the structure below. (I 4/AC) CH3 L19. Provide a name for the compound below. CAPAC) CH3 CH,CECCHCH2CH2CH3 50. Provide the correct IUPAC name for the following compound. NO2 CH 51. Give an acceptable name for the following substance. IUPAC HOCH,CH OH Name: S7 Provide the IUPAC name for the structure below. H NOZ 53. Provide the IUPAC name for the following structure. OH ОН 54 Draw a structure corresponding to the following IUPAC name. diethyl...
1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3 pts.) 2. Draw the bond-line structure of (2,4Z)-2,5-dibromo-3-methylhexa-2,4-diene. (3 pts.) 3. Label the most stable and the least stable alkene (4 pts.) 4. Consider the substitution reaction below. (4 pts.) NaSH DMF SH in why this reaction proceeds through an SN mechanism and not an S2 mechanism a) Explain why this reaction proces o b) Explain why this reaction produces a racemic mixture of...
1. Follow the instructions given: 20 points. a. Provide the IUPAC name for the molecule shown below. (4 points) b. Provide the IUPAC name for the molecule shown below. (4 points) c. Of the cations shown below, circle any that are chiral. (4 points) d. Draw the expected product of the reaction below and briefly explain why three, not two equivalents of NaNH2 are required. (5 points) Br- 3 NaNH2 NH e. Rank the following radicals in terms of their...
Compound A Compound B Give the IUPAC name for Compound A. 2. Give the IUPAC name for Compound B. 3. Which compound from above (Compound A or Compound B) is more soluble in water and why? 4. Which compound can be dehydrated to form a double bond (Compound A or Compound B)? Draw the most likely product of that dehydration. (Insert a picture of your drawing of the molecule or a scan of your drawing of the molecule) 5. Could...
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