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1. Consider the nomenclature of amines: (a) Write the IUPAC and/or common name for the following...
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correc name...
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correc name doesn't appear, choose "none of the above." (3 pts each) a. 2-butyl-2-methylepoxide b. 1,2-epoxy-2-methylbutane c.2-butyl-2-methyloxirane d. 1,2-epoxy-2-methylpropane e. none of the above a. 1-ethoxy-2-isopropyl ether b. ethyl isobutyl ether c. 1-ethyl-2-methylbutane d. 1-ethoxy-2-isobutyl ether e. none of the above 3. I a. 1-sec-butyl-2-methylcyclopentene b. 1-iso-butyl-2-methylcyclopentane c. 1-methyl-2-sec-butylcyclopentene d. 1-sec-butyl-2-methylcyclohexene e, none of the above 4. Provide the structure for pyridine in the box below:...
8.A compound has the common name N-methylbenzamide. Which of the following is not true? Question 8...
8.A compound has the common name N-methylbenzamide. Which of the following is not true? Question 8 options: N-methylbenzamide must include an aromatic benzene ring N-methylbenzamide contains nitrogen N-methylbenzamide has a carbonyl C=O and nitrogen, therefore is an amide Since N-methylbenzamide has a methyl bonded to nitrogen it must be a secondary amine 9.Which of these types of compounds forms salts with acids? Question 9 options: alcohols amines ethers ketones 10. All of the following are properties of amines except: Question...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: WHICHCH2 at CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadienc (3Z,SE) -2,6-dimethyl-1,3,5,7-octatetraene 4-methyl-1.2-hexadiene
please solve both 3. Name the following alkylamine, aniline and N-substituted amines: sec-Butylamine C D Butylamine...
please solve both
3. Name the following alkylamine, aniline and N-substituted amines: sec-Butylamine C D Butylamine Isobutylamine Propylamine 1-Methyl-1-phenylethylamine 1-Phenylethylamine _C _D 1-Methyl-l-phenylpropylamine 2-Bhenylethylamine 3/8 A 2-Fluoro-5-(sec-butyl)aniline S-Fluoro-2-(sec-butyl)aniline _B _ D 2-Fluoro-5-isobutyl aniline -Fluoro-2-isobutyl)aniline S N-Propylethylamine N-Ethylbutylamine _B _D N-Ethylpropylamine N-Ethylisopropyl)amine _B 1-N-Methyl-1-l-ethylcyclohex-l yl)amine 1-N-Ethyl-1-1-methylcyclohex-1- vljamine 1. N-Ethyl-1-cyclohex-1-ylamine 1-N-Ethyl-1-N-methyl-1-cyclohex-1- vlamine 4. Complete the acid-base equilibrium reactions below by filling in the boxes. Show the flow of electrons with curly arrows and indicate on which side the equilibrium lies by drawing...
COURSE TITE & CODE-Organic Chemistry-II (CHEM3201) EXERCISE NO-1 Exercise: 1. How is classification of amines different...
COURSE TITE & CODE-Organic Chemistry-II (CHEM3201) EXERCISE NO-1 Exercise: 1. How is classification of amines different from that of alcohols? Exercise: 2. Amines are more basic than comparable alcohols. Exercise: 3. How will you distinguish between (a) Aniline and methyl amine (b) Di-methyl amine and tri-methyl amine. Exercise: 4. Write structure and IUPAC name of The amide which gives propanamine by Hofmann bromamide reaction (ii) The salt which gives methylene cyclohexene & trimethylamine by the Hoffman elimination reaction. Exercise: 5....
3. 12 pts. Draw the structural formula for the following amines and amides: a. Diethylamine &n
3. 12 pts. Draw the structural formula for the following amines and amides: a. Diethylamine d. 2-amino-4-hydroxy heptane b. 3-methyl aniline e. N-methyl-1-amino pentane c. 3-amino-3-methyl-2-hexanol f. propanamide 4. 3 pts. Write out the chemical reaction of ethyl amine with HCl. Use the structural formula for the reactant and product. Name the product. 5. 3 pts. Write out the structures and complete the reaction for: 1-amino pentane + HCl
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correct name...
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correct name doesn't appear, choose "none of the above." (3 pts each) 1 HO, H HO H a. (2R 3R)-2,3-butanediol b. (2R 3R)-butane-2,3-diol c. (25,3R)-butane-2,3-diol d. (25,3R)-2,3-butanediol e. none of the above vo a. 1-ethoxy-3-ethylheptane b. 7-ethoxy-5-ethylheptane c. 5-ethyl-5-propoxyheptane d. 3-ethyl-1-ethoxyheptane e. none of the above a. (2E)-2-methyl-6-Isopropyl-heptene b. (2E)-3-isopropyl-2-heptene C. (22)-5-isopropyl-6-heptene d. (22)-3-isopropyl-2-heptene e, none of the above co a. 1,2-epoxy-1,1,3-trimethylcyclohexane b. 1,2-epoxy-1,3,3-trimethylcyclohexane c.1-epoxide-1,3,3-trimethylcyclohexane d....
(3 pts each, unless otherwise noted, 17 pts total) 1-5. Nomenclature: provide an acceptable name for...
(3 pts each, unless otherwise noted, 17 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following compounds, but do NOT Google. 1. 2. 3. -CO No HN -CO,H COM 5. (5 pts) Name IUPAC ONLY. i HN-CHE H-C-N(CH)2 (4 pts each, unless otherwise noted, 16 pts total) 6-9. Structures: provide an acceptable structure for: 6. the isobutyl diester of B-bromopimelic acid (5 pts) 7. N-ethyl-B-ethyl-y-valerylactam. 8. benzoic B-chloropropionic anhydride (3 pts) 9. o-bromobenzoyl chloride
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC...
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 CHCH Il III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1.5-octadiene 4-methyl-12-hekadiene (3ZSE) -2,6-dimethyl-1.3.5.7-octaterne
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correc name doesn't appear, choose "none of the above." (3 pts each) a. 2-butyl-2-methylepoxide b. 1,2-epoxy-2-methylbutane c.2-butyl-2-methyloxirane d. 1,2-epoxy-2-methylpropane e. none of the above a. 1-ethoxy-2-isopropyl ether b. ethyl isobutyl ether c. 1-ethyl-2-methylbutane d. 1-ethoxy-2-isobutyl ether e. none of the above 3. I a. 1-sec-butyl-2-methylcyclopentene b. 1-iso-butyl-2-methylcyclopentane c. 1-methyl-2-sec-butylcyclopentene d. 1-sec-butyl-2-methylcyclohexene e, none of the above 4. Provide the structure for pyridine in the box below:...
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 a CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadiene (3Z,SE) -26-dimethyl-1,3,5,7-octatetraene 4-methyl-1,2-hexadiene
Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: WHICHCH2 at CHCH2 II III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1,5-octadienc (3Z,SE) -2,6-dimethyl-1,3,5,7-octatetraene 4-methyl-1.2-hexadiene
please solve both
3. Name the following alkylamine, aniline and N-substituted amines: sec-Butylamine C D Butylamine Isobutylamine Propylamine 1-Methyl-1-phenylethylamine 1-Phenylethylamine _C _D 1-Methyl-l-phenylpropylamine 2-Bhenylethylamine 3/8 A 2-Fluoro-5-(sec-butyl)aniline S-Fluoro-2-(sec-butyl)aniline _B _ D 2-Fluoro-5-isobutyl aniline -Fluoro-2-isobutyl)aniline S N-Propylethylamine N-Ethylbutylamine _B _D N-Ethylpropylamine N-Ethylisopropyl)amine _B 1-N-Methyl-1-l-ethylcyclohex-l yl)amine 1-N-Ethyl-1-1-methylcyclohex-1- vljamine 1. N-Ethyl-1-cyclohex-1-ylamine 1-N-Ethyl-1-N-methyl-1-cyclohex-1- vlamine 4. Complete the acid-base equilibrium reactions below by filling in the boxes. Show the flow of electrons with curly arrows and indicate on which side the equilibrium lies by drawing...
COURSE TITE & CODE-Organic Chemistry-II (CHEM3201) EXERCISE NO-1 Exercise: 1. How is classification of amines different from that of alcohols? Exercise: 2. Amines are more basic than comparable alcohols. Exercise: 3. How will you distinguish between (a) Aniline and methyl amine (b) Di-methyl amine and tri-methyl amine. Exercise: 4. Write structure and IUPAC name of The amide which gives propanamine by Hofmann bromamide reaction (ii) The salt which gives methylene cyclohexene & trimethylamine by the Hoffman elimination reaction. Exercise: 5....
NOMENCLATURE: Choose the correct IUPAC name for each of the structures below. If the correct name doesn't appear, choose "none of the above." (3 pts each) 1 HO, H HO H a. (2R 3R)-2,3-butanediol b. (2R 3R)-butane-2,3-diol c. (25,3R)-butane-2,3-diol d. (25,3R)-2,3-butanediol e. none of the above vo a. 1-ethoxy-3-ethylheptane b. 7-ethoxy-5-ethylheptane c. 5-ethyl-5-propoxyheptane d. 3-ethyl-1-ethoxyheptane e. none of the above a. (2E)-2-methyl-6-Isopropyl-heptene b. (2E)-3-isopropyl-2-heptene C. (22)-5-isopropyl-6-heptene d. (22)-3-isopropyl-2-heptene e, none of the above co a. 1,2-epoxy-1,1,3-trimethylcyclohexane b. 1,2-epoxy-1,3,3-trimethylcyclohexane c.1-epoxide-1,3,3-trimethylcyclohexane d....
(3 pts each, unless otherwise noted, 17 pts total) 1-5. Nomenclature: provide an acceptable name for each of the following compounds, but do NOT Google. 1. 2. 3. -CO No HN -CO,H COM 5. (5 pts) Name IUPAC ONLY. i HN-CHE H-C-N(CH)2 (4 pts each, unless otherwise noted, 16 pts total) 6-9. Structures: provide an acceptable structure for: 6. the isobutyl diester of B-bromopimelic acid (5 pts) 7. N-ethyl-B-ethyl-y-valerylactam. 8. benzoic B-chloropropionic anhydride (3 pts) 9. o-bromobenzoyl chloride
VL Nomenclature: Name and draw the structures of the following organic molecules: 1) Give the IUPAC name of the following compounds: CHCH2 CHCH Il III 2) Drawing Structures Methylenecyclohexane Trans-3,3-dimethyl-4-propyl-1.5-octadiene 4-methyl-12-hekadiene (3ZSE) -2,6-dimethyl-1.3.5.7-octaterne
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