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1. The structures of six organic compounds are shown below. HEH (6) 9 NHE (d) (e)...
1. The structures of six organic compounds are shown below. NHE (i) Give the name(s) of...
1. The structures of six organic compounds are shown below. NHE (i) Give the name(s) of the functional group(s) in each compound. All compounds have at least one functional group; some ha ve more than one. (ii) Give the letter(s) of the compound(s) that are aromatic. Write "None" if there are no aromatic compounds. (iii) Give the letter(s) of the compound(s) that have optical isomers. Write "None" if no compound has optical isomers. (iv) What is the molecular formula of...
1.The structures of six organic compounds are shown below H2 0 он functional group compounds. has...
1.The structures of six organic compounds are shown below H2 0 он functional group compounds. has optical isomers. (i) Give the name(s) of the functional group s) in each compound. All compounds have at least one (ii) Give the letter(s) of the compound(s) that are aromatic. Write "None" if there are no aromatic (iii) Give the letter(s) of the compound(s) that have optical isomers. Write "None" if no compound (iv) What is the molecular formula of (c)? : some hav...
5. Six compounds shown below (A-F) have molecular formula C H202. Answer the following questions. (8...
5. Six compounds shown below (A-F) have molecular formula C H202. Answer the following questions. (8 points) OH a. Indicate two isomers that are enantiomers of each other: b. Indicate two isomers that are diastereomers of each other: c. Indicate two structures that are identical: d. Indicate a meso compound:
s appear/look differently. This can often be The maie and female of the same specie to...
s appear/look differently. This can often be The maie and female of the same specie to the presence and/or position of functional groups 7. d. none of the above c. sexual dimorphism with their descriptions: 8-12. Match the following functional groups as their functional group 8. Alcohols have 9. Acetic acid (organic acids) have 10. Proteins/amino acids have as their functional grou as one of their functional groups 11. Thiols have 12. An organic compound with-CO at the end of...
Hints for identifying compounds in multiple-choice problems (problems 1:5); 1. Closely compare the given compounds. Determine...
Hints for identifying compounds in multiple-choice problems (problems 1:5); 1. Closely compare the given compounds. Determine which piece of information (molecular weight from MS, number of peaks in the NMR, presence of a special functional group in the IR, etc) would be the easiest for distinguishing between the given compounds. You might not need to use all types of given spectra to find your correct compound! 2. Based on your answer from step 1, consult the appropriate spectrum first. For...
vii) Two organic compounds which have the same molecular formula but different structural formula are called...
vii) Two organic compounds which have the same molecular formula but different structural formula are called _____ ix. Open chain organic compounds are called _____ x. The family of hydrocarbons whose molecules have double or triple bond between carbon atoms is called _____ xi. An atom or a group of atoms which give characteristic properties to an organic compound are called _____ xii. The organic compounds which contain only Hydrogen and Carbon are called _____ What is the pH of...
Analyze each pair of compounds structures represent. Your cho cach pair of compounds below. Identify which...
Analyze each pair of compounds structures represent. Your cho cach pair of compounds below. Identify which class of isomers each pair of s represent. Your choices are: (i) constitutional, (ii) conformational, (iii) omers, (iv) diastereomer or (v) identical (non-isomers). Only one label for each pair should be used. For each case show work (drawings, (R)/(S), rotation of bonds, chair- "ps, etc) which led you to each answer for the pairs below. Any differences of answers between you and your peers...
9 & 10. Treatment of the optically pure (S)- cyclohexanone (1) shown below with sodium methane...
9 & 10. Treatment of the optically pure (S)- cyclohexanone (1) shown below with sodium methane thiolate in THF (tetrahydrofuran the solvent) gives products A and B that both have the same molecular formula CgH14SO. Compound A and B are easily physically separated by distillation with A having the lower boiling point and it is found that the optical rotation of the purified and separated substances A and B [ajo 0. It is experimentally found that the rate of formation...
PART I: HYDRIDES AND PERIODICITY Table 10-1. Lewis structures of hydrides Formula Total # of Valence...
PART I: HYDRIDES AND PERIODICITY Table 10-1. Lewis structures of hydrides Formula Total # of Valence Central Atom of Hydride Electrons Lewis Structure S aloon loro p ro bono di non auto Sad Ind o nesboro both bobom Table 10-2. Molecular geometries w of Lone Electron Electron-Pair Pairs Geometry Central Atom # of Bonded Electron Pairs Formula of Hydride Bond Angles) Molecular Shape ci TA's Initials PART II. FLUORINATED COMPOUNDS Table 10-3. Fluorinated compounds Total # of E. Pairs around...
Need help understanding what compounds to use when doing multistep syntheses. 5. (Multistep synthesis) For each...
Need help understanding what compounds to use when doing
multistep syntheses.
5. (Multistep synthesis) For each of the following multistep syntheses, provide an efficient multistep synthesis of the target compound from the starting compound. More than one reaction is required for this synthesis. You may use any inorganic compounds that you need. For cach functional group transformation, give all necessary reagents, solvents, and catalysts; give a structural formula of the organic reactant and the major organic product(s). Show stercochemistry appropriately...
1. The structures of six organic compounds are shown below. NHE (i) Give the name(s) of the functional group(s) in each compound. All compounds have at least one functional group; some ha ve more than one. (ii) Give the letter(s) of the compound(s) that are aromatic. Write "None" if there are no aromatic compounds. (iii) Give the letter(s) of the compound(s) that have optical isomers. Write "None" if no compound has optical isomers. (iv) What is the molecular formula of...
1.The structures of six organic compounds are shown below H2 0 он functional group compounds. has optical isomers. (i) Give the name(s) of the functional group s) in each compound. All compounds have at least one (ii) Give the letter(s) of the compound(s) that are aromatic. Write "None" if there are no aromatic (iii) Give the letter(s) of the compound(s) that have optical isomers. Write "None" if no compound (iv) What is the molecular formula of (c)? : some hav...
5. Six compounds shown below (A-F) have molecular formula C H202. Answer the following questions. (8 points) OH a. Indicate two isomers that are enantiomers of each other: b. Indicate two isomers that are diastereomers of each other: c. Indicate two structures that are identical: d. Indicate a meso compound:
s appear/look differently. This can often be The maie and female of the same specie to the presence and/or position of functional groups 7. d. none of the above c. sexual dimorphism with their descriptions: 8-12. Match the following functional groups as their functional group 8. Alcohols have 9. Acetic acid (organic acids) have 10. Proteins/amino acids have as their functional grou as one of their functional groups 11. Thiols have 12. An organic compound with-CO at the end of...
Hints for identifying compounds in multiple-choice problems (problems 1:5); 1. Closely compare the given compounds. Determine which piece of information (molecular weight from MS, number of peaks in the NMR, presence of a special functional group in the IR, etc) would be the easiest for distinguishing between the given compounds. You might not need to use all types of given spectra to find your correct compound! 2. Based on your answer from step 1, consult the appropriate spectrum first. For...
vii) Two organic compounds which have the same molecular formula but different structural formula are called _____ ix. Open chain organic compounds are called _____ x. The family of hydrocarbons whose molecules have double or triple bond between carbon atoms is called _____ xi. An atom or a group of atoms which give characteristic properties to an organic compound are called _____ xii. The organic compounds which contain only Hydrogen and Carbon are called _____ What is the pH of...
Analyze each pair of compounds structures represent. Your cho cach pair of compounds below. Identify which class of isomers each pair of s represent. Your choices are: (i) constitutional, (ii) conformational, (iii) omers, (iv) diastereomer or (v) identical (non-isomers). Only one label for each pair should be used. For each case show work (drawings, (R)/(S), rotation of bonds, chair- "ps, etc) which led you to each answer for the pairs below. Any differences of answers between you and your peers...
9 & 10. Treatment of the optically pure (S)- cyclohexanone (1) shown below with sodium methane thiolate in THF (tetrahydrofuran the solvent) gives products A and B that both have the same molecular formula CgH14SO. Compound A and B are easily physically separated by distillation with A having the lower boiling point and it is found that the optical rotation of the purified and separated substances A and B [ajo 0. It is experimentally found that the rate of formation...
PART I: HYDRIDES AND PERIODICITY Table 10-1. Lewis structures of hydrides Formula Total # of Valence Central Atom of Hydride Electrons Lewis Structure S aloon loro p ro bono di non auto Sad Ind o nesboro both bobom Table 10-2. Molecular geometries w of Lone Electron Electron-Pair Pairs Geometry Central Atom # of Bonded Electron Pairs Formula of Hydride Bond Angles) Molecular Shape ci TA's Initials PART II. FLUORINATED COMPOUNDS Table 10-3. Fluorinated compounds Total # of E. Pairs around...
Need help understanding what compounds to use when doing
multistep syntheses.
5. (Multistep synthesis) For each of the following multistep syntheses, provide an efficient multistep synthesis of the target compound from the starting compound. More than one reaction is required for this synthesis. You may use any inorganic compounds that you need. For cach functional group transformation, give all necessary reagents, solvents, and catalysts; give a structural formula of the organic reactant and the major organic product(s). Show stercochemistry appropriately...
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