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D Question 22 6 pts Which of the following is the correct name for the compound...
What is the IUPAC name of the following compound? propane O 6-chloro-7-methyl-3-propyloctan-2-ol O (3R, 7R)-7-bromo-3-chloro-1-methylhept-1-ene O...
What is the IUPAC name of the following compound? propane O 6-chloro-7-methyl-3-propyloctan-2-ol O (3R, 7R)-7-bromo-3-chloro-1-methylhept-1-ene O (3R, 6E)-5-isopropyl-4-propyloct-6-en-3-ol O (55, 6E)-4-sec-butyl-5-chlorodec-6-en-2-yne Today is Graduation for many fellow FSU students. On these days, many individuals enjoy celebratory beverages such as champagne, wine, beer, and other spirits. Each of these have a singular common organic molecule whose presence requires consumers to be at least 21 years of age in the U.S.. Which of the following molecules that you learned in organic I...
Find correct name CHE 2434 Test Mark the best answer on a scantron, do not write...
Find correct name
CHE 2434 Test Mark the best answer on a scantron, do not write on this test MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question 1) What is the correct IUPAC name for the following structure 1) A) 2) 1-cyclopentyl-3,6-dimethylhept-3-en-1-yne B) (0) 1-cyclopentyl-3,6-dimethylhept-3-en-1-yne C) )1-cyclopentyl-4,7-dimethylhept-4-en-2-yne D) 0) 1-cyclopentyl-3,6-dimethylhept-1-yn-3-em 2) Provide the IUPAC name for the compound below 2) (HC)HCCECCH.CI A) 5-chloro-2-methylpent-3-yne C) sec-butylchloromethylacetylene B) 1-chloro-4,4-dimethylbut-2-yne D) 1-chloro-4-methylpent-2-yne 3) The correct IUPAC...
help with number 6 would be great D) (S,E)-3-bromo-4-methylhex-2-ene R, E)-3-bromo-4-met hylhex-2-ene 5. Name the following...
help with number 6 would be great
D) (S,E)-3-bromo-4-methylhex-2-ene R, E)-3-bromo-4-met hylhex-2-ene 5. Name the following compound: A (SE)-3-chlorohex-4-en-1-yne DA (R,E)-3-chlorohex-2-en-5-yne C) (S,E)-3-chlorohex-2-en-5-yne DA (R,E)-3-chlorohex-4-en-1-yne Cl (RE)-3-chloropent-4-en-1-yne 6. Which molecule would have the lowest heat of hydrogenation? IV A) 1 B)Il C)III D) IV E)V
1. Give the correct name for each compound. 2. Determine the degree of unsaturation for the...
1. Give the correct name for each compound. 2. Determine the degree of unsaturation for the molecular formula, C.H.BrCl. Draw and name at least five isomers for the above molecular formula. 3. Draw a structure for each compound. (a) (E)-2-chloro-2-hexene (b) (3,6Z)-1,3,6-octatriene (c) trans-3-methylhept-3-ene 4. Predict the elimination product(s) formed by debromination of the following compound with iodide ion in acetone. Include stereochemistry, and give a correct name for the product. B -CH₃ "Br + Acetone r A CH₂ 5....
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid...
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid e) (3S,4S,5S)-5-amino-3-hydroxy-4-methylhexanal f) (Z,2R,4R)-6-bromo-4-chloro-N-ethyl-N-methylhept-5-en-2-amine g) [(1S)-1-chloroethyl] (Z,3R)-5-chloro-3-methoxyhex-4-enoate h) (Z,3R)-3-bromo-4-chloro-7-methyloct-4-enoic acid i) (3S)-6-bromo-N-ethyl-N,3-dimethylhex-4-ynamide j) (Z,3R,4S)-6-bromo-3-[(1S)-1-chloroethyl]-4-hydroxyhept-5-en-2-one
HELP tatMtiele Cheice 2.0peints.each Which of the fellowing structures is mest stable? How many stereaisomers does...
HELP
tatMtiele Cheice 2.0peints.each Which of the fellowing structures is mest stable? How many stereaisomers does the molecule below have? 2) CH)HCtCH CHCH CH3 CH2 br OH e) 9 d) 8 c) 6 b)4 al 3 Which of the follewing molecules below are chiral? 3) HO Ho e) 1, 2 and 3 a) Only 1 d) 1 and 3 b) 1 and 3 c) 2 and 3 What is the relationship between the following two compounds? 4 сн, H- H...
Which of the following structures is most stable? 2) How many stereoisomers does the molecule below...
Which of the following structures is most stable? 2) How many stereoisomers does the molecule below have? (СН), С+ снен снаси сна OH CH₃ br. a) 3 6) 4 c) 6 d) 8 e 9 3) Which of the following molecules below are chiral? 0) to A Boh A MOH HOS DBr e) 1, 2 and 3 a) Only 1 b) 1 and 3 c) 2 and 3 d) 1 and 3 What is the relationship between the following two...
Which is the correct name for the compound shown below? H. O (2R,35)-2-Bromo-3-chlorobutane (25,3R)-2-Bromo-3-chlorobutane (2R, 3R)-2-Bromo-3-chlorobutane...
Which is the correct name for the compound shown below? H. O (2R,35)-2-Bromo-3-chlorobutane (25,3R)-2-Bromo-3-chlorobutane (2R, 3R)-2-Bromo-3-chlorobutane (2S,3S)-2-Bromo-3-chlorobutane Which compound is achiral? O meso-2,5-Difluorohexane O trans-1,2-Dimethylcyclohexane O (S)-3-lodohexane (2R, 3R)-2,3-Dibromoheptane 1
help with question #7 pts) 1. Give the IUPAC name for the following compound: NH OH...
help with question #7
pts) 1. Give the IUPAC name for the following compound: NH OH H3 CH-CH2-CH-CH2-CH, D 5-amino-3-Hexanol amn 4 3 2 2 pts) 2. Draw the structural formula for 2-amino-3-oxo-pentanal. H-CH₂-CH₂-C- CH₂ - CH3 2 pts) 3. Write the balanced chemical equation (using structural formulas) for the lissociation of diethylamine in water. CH₃-CH₂-N-CH₂-CH₃ + H₂O -> CH₃-CH ₂ - N - CH₂ +OH-CH3 CAN- | CH-CH2N-CH, - Lidocaine (Xylocaine) 3 pts) 4. Lidocaine (Xylocaine) is used as...
10) Which of the following statements is (are) true for the compound (R)-2-butanol? A) This compound...
10) Which of the following statements is (are) true for the compound (R)-2-butanol? A) This compound is chiral. B) This compound is optically active. C) This compound has an enantiomer D) all of the above E) none of the above 11) Predict the specific rotation of the compound shown. CH нс A) It is impossible to predict; it must be determined experimentally. B) Because both asymmetric centers are R, the compound is dextrorotatory. C) Because both asymmetric centers are S,...
What is the IUPAC name of the following compound? propane O 6-chloro-7-methyl-3-propyloctan-2-ol O (3R, 7R)-7-bromo-3-chloro-1-methylhept-1-ene O (3R, 6E)-5-isopropyl-4-propyloct-6-en-3-ol O (55, 6E)-4-sec-butyl-5-chlorodec-6-en-2-yne Today is Graduation for many fellow FSU students. On these days, many individuals enjoy celebratory beverages such as champagne, wine, beer, and other spirits. Each of these have a singular common organic molecule whose presence requires consumers to be at least 21 years of age in the U.S.. Which of the following molecules that you learned in organic I...
Find correct name
CHE 2434 Test Mark the best answer on a scantron, do not write on this test MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question 1) What is the correct IUPAC name for the following structure 1) A) 2) 1-cyclopentyl-3,6-dimethylhept-3-en-1-yne B) (0) 1-cyclopentyl-3,6-dimethylhept-3-en-1-yne C) )1-cyclopentyl-4,7-dimethylhept-4-en-2-yne D) 0) 1-cyclopentyl-3,6-dimethylhept-1-yn-3-em 2) Provide the IUPAC name for the compound below 2) (HC)HCCECCH.CI A) 5-chloro-2-methylpent-3-yne C) sec-butylchloromethylacetylene B) 1-chloro-4,4-dimethylbut-2-yne D) 1-chloro-4-methylpent-2-yne 3) The correct IUPAC...
help with number 6 would be great
D) (S,E)-3-bromo-4-methylhex-2-ene R, E)-3-bromo-4-met hylhex-2-ene 5. Name the following compound: A (SE)-3-chlorohex-4-en-1-yne DA (R,E)-3-chlorohex-2-en-5-yne C) (S,E)-3-chlorohex-2-en-5-yne DA (R,E)-3-chlorohex-4-en-1-yne Cl (RE)-3-chloropent-4-en-1-yne 6. Which molecule would have the lowest heat of hydrogenation? IV A) 1 B)Il C)III D) IV E)V
1. Give the correct name for each compound. 2. Determine the degree of unsaturation for the molecular formula, C.H.BrCl. Draw and name at least five isomers for the above molecular formula. 3. Draw a structure for each compound. (a) (E)-2-chloro-2-hexene (b) (3,6Z)-1,3,6-octatriene (c) trans-3-methylhept-3-ene 4. Predict the elimination product(s) formed by debromination of the following compound with iodide ion in acetone. Include stereochemistry, and give a correct name for the product. B -CH₃ "Br + Acetone r A CH₂ 5....
HELP
tatMtiele Cheice 2.0peints.each Which of the fellowing structures is mest stable? How many stereaisomers does the molecule below have? 2) CH)HCtCH CHCH CH3 CH2 br OH e) 9 d) 8 c) 6 b)4 al 3 Which of the follewing molecules below are chiral? 3) HO Ho e) 1, 2 and 3 a) Only 1 d) 1 and 3 b) 1 and 3 c) 2 and 3 What is the relationship between the following two compounds? 4 сн, H- H...
Which of the following structures is most stable? 2) How many stereoisomers does the molecule below have? (СН), С+ снен снаси сна OH CH₃ br. a) 3 6) 4 c) 6 d) 8 e 9 3) Which of the following molecules below are chiral? 0) to A Boh A MOH HOS DBr e) 1, 2 and 3 a) Only 1 b) 1 and 3 c) 2 and 3 d) 1 and 3 What is the relationship between the following two...
Which is the correct name for the compound shown below? H. O (2R,35)-2-Bromo-3-chlorobutane (25,3R)-2-Bromo-3-chlorobutane (2R, 3R)-2-Bromo-3-chlorobutane (2S,3S)-2-Bromo-3-chlorobutane Which compound is achiral? O meso-2,5-Difluorohexane O trans-1,2-Dimethylcyclohexane O (S)-3-lodohexane (2R, 3R)-2,3-Dibromoheptane 1
help with question #7
pts) 1. Give the IUPAC name for the following compound: NH OH H3 CH-CH2-CH-CH2-CH, D 5-amino-3-Hexanol amn 4 3 2 2 pts) 2. Draw the structural formula for 2-amino-3-oxo-pentanal. H-CH₂-CH₂-C- CH₂ - CH3 2 pts) 3. Write the balanced chemical equation (using structural formulas) for the lissociation of diethylamine in water. CH₃-CH₂-N-CH₂-CH₃ + H₂O -> CH₃-CH ₂ - N - CH₂ +OH-CH3 CAN- | CH-CH2N-CH, - Lidocaine (Xylocaine) 3 pts) 4. Lidocaine (Xylocaine) is used as...
10) Which of the following statements is (are) true for the compound (R)-2-butanol? A) This compound is chiral. B) This compound is optically active. C) This compound has an enantiomer D) all of the above E) none of the above 11) Predict the specific rotation of the compound shown. CH нс A) It is impossible to predict; it must be determined experimentally. B) Because both asymmetric centers are R, the compound is dextrorotatory. C) Because both asymmetric centers are S,...
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