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7. The IUPAC name for the followe d in the OH controls a) 3-chloro-2-methylcyclohexanol 5-chloro-2-methylcyclohexanol 2-methyl-3-chlorocyclohexanol...
7. The IUPAC name for the he IUPAC name for the following compound is: hint: the...
7. The IUPAC name for the he IUPAC name for the following compound is: hint: the OH controls the name a) 3-chloro-2-methylcyclohexanol b) 1-chloro-4-methylcyclohexanol c) 2-methyl-3-chlorocyclohexanol d) 2-methyl-5-chlorocyclohexanol e) 5-chloro-2-methylcyclohexanol 8. Which of the following cannot be an electrophile? b) BF, c) *NO d) Fel a) H e ) CH2=CH, BF 9. Based on the following energy diagram, which compound is formed faster? Reacton a) A from B b ) B from A c) Cfrom 8 d) CB from C...
draw fisher projections for both the D and L isomers of the following 12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O...
draw fisher projections for both the D and L isomers of the
following
12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O он HOH HOH но CH,OH CH,OH 3 Draw Fischer projections for both the D and L isomers of the following a. 2,3-dihydroxypropanoic acid b. 2-chloro-3-hydroxypropanoic acid Draw Fischer projections for both the D and L somers of the following amino acids:...
Based on the energy diagram below, the free energY of the reaction is represented as 13....
Based on the energy diagram below, the free energY of the reaction is represented as 13. de Energy C. Reaction Progness e) A-B A b) в d) D 14. The addition of a reagent to the si face of the a compound will produce a) An S enantiomer c) A racemic mixture b) An R enantiomer d) A meso compound e) An achiral compound How many chirality centers are present in the compound below? 15. C1 a) 1 b) 2...
7. What is the relationship between these two compounds? CHO CH OH H HH HE A....
7. What is the relationship between these two compounds? CHO CH OH H HH HE A. The compounds are identical. B. The compounds are enantiomers. C. The compounds are diastereomers. D. The compounds are structural isomers. нонс OHC 8 What is the relationship between these two compounds? соон COOH H- ci CH A. The compounds are identical. B. The compounds are enantiomers. C. The compounds are diastereomers. D. The compounds are structural isomers. CH CH3 CH,OH CH, OH 9. What...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8....
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
i need both questions please Dehydration of 2 Methyl Cyclohexanol: OH CH CHE H2PO4 2-methylcyclohexanol C...
i need both questions please
Dehydration of 2 Methyl Cyclohexanol: OH CH CHE H2PO4 2-methylcyclohexanol C H140 Mol. Wt.: 114.19 1-methylcyclohex-1-ene CH2 Mol. Wt: 96.17 7. (15 pts) Draw the experiment setup of this experiment and label each piece of equipment used. 8. (10 pts) Draw out the mechanism of the above reaction
2). Consider the following intramolecular S2 reaction. no ♡ + HI A) (5 pts) Use the...
2). Consider the following intramolecular S2 reaction. no ♡ + HI A) (5 pts) Use the table of Bond Dissociation Enthalpies (at the back of the exam) to calculate the approximate ΔΗπη. B) (3 pts) Is the reaction endothermic or exothermic? Why? C) (6 pts) Draw the Reaction Energy Coordinate Diagram. Label the axes, reactant(s), product(s), transition state(s), intermediate(s), activation energy, and reaction enthalpy. D) (3 pts) In regards to entropy, would you expect the reaction to be favorable, or...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH OH OH c. 3 d. 4 Que. 10) What is the relationship between D-erythrose and D-threose? CHO CHO HOH HOH H OH OH CHOH CH,OH D-Erythrose D-Threose a. constitutional isomers b. enantiomers c. diastereomers d. tautomers Que. 11) What is the relationship between D-ribose and D-xylose? CHO CHO І н он н -он нон нон н -он н -он І І CH OH Сн,он...
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...
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol...
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol c. 5,5-diethyl-1-heptanol d. 2-ethyl-4-isopropylcyclohexanol e. 4-ethylphenol f. 2-nitrophenol g. cyclopropyl methyl ether h. isopropyl propyl ether 8.2 Give the product for the dehydration of each of the following alcohols. CH-CH2-CH3 a. ОН b. ОН C. OH d. 8.3 What product would result from the oxidation of each of the following alcohols? Write the chemical equations. a. 2-butanol b. 2-methyl-2-pentanol c. cyclohexanol d. 3-ethylcyclopentanol Name...
7. The IUPAC name for the he IUPAC name for the following compound is: hint: the OH controls the name a) 3-chloro-2-methylcyclohexanol b) 1-chloro-4-methylcyclohexanol c) 2-methyl-3-chlorocyclohexanol d) 2-methyl-5-chlorocyclohexanol e) 5-chloro-2-methylcyclohexanol 8. Which of the following cannot be an electrophile? b) BF, c) *NO d) Fel a) H e ) CH2=CH, BF 9. Based on the following energy diagram, which compound is formed faster? Reacton a) A from B b ) B from A c) Cfrom 8 d) CB from C...
draw fisher projections for both the D and L isomers of the
following
12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O он HOH HOH но CH,OH CH,OH 3 Draw Fischer projections for both the D and L isomers of the following a. 2,3-dihydroxypropanoic acid b. 2-chloro-3-hydroxypropanoic acid Draw Fischer projections for both the D and L somers of the following amino acids:...
Based on the energy diagram below, the free energY of the reaction is represented as 13. de Energy C. Reaction Progness e) A-B A b) в d) D 14. The addition of a reagent to the si face of the a compound will produce a) An S enantiomer c) A racemic mixture b) An R enantiomer d) A meso compound e) An achiral compound How many chirality centers are present in the compound below? 15. C1 a) 1 b) 2...
7. What is the relationship between these two compounds? CHO CH OH H HH HE A. The compounds are identical. B. The compounds are enantiomers. C. The compounds are diastereomers. D. The compounds are structural isomers. нонс OHC 8 What is the relationship between these two compounds? соон COOH H- ci CH A. The compounds are identical. B. The compounds are enantiomers. C. The compounds are diastereomers. D. The compounds are structural isomers. CH CH3 CH,OH CH, OH 9. What...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
i need both questions please
Dehydration of 2 Methyl Cyclohexanol: OH CH CHE H2PO4 2-methylcyclohexanol C H140 Mol. Wt.: 114.19 1-methylcyclohex-1-ene CH2 Mol. Wt: 96.17 7. (15 pts) Draw the experiment setup of this experiment and label each piece of equipment used. 8. (10 pts) Draw out the mechanism of the above reaction
2). Consider the following intramolecular S2 reaction. no ♡ + HI A) (5 pts) Use the table of Bond Dissociation Enthalpies (at the back of the exam) to calculate the approximate ΔΗπη. B) (3 pts) Is the reaction endothermic or exothermic? Why? C) (6 pts) Draw the Reaction Energy Coordinate Diagram. Label the axes, reactant(s), product(s), transition state(s), intermediate(s), activation energy, and reaction enthalpy. D) (3 pts) In regards to entropy, would you expect the reaction to be favorable, or...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH OH OH c. 3 d. 4 Que. 10) What is the relationship between D-erythrose and D-threose? CHO CHO HOH HOH H OH OH CHOH CH,OH D-Erythrose D-Threose a. constitutional isomers b. enantiomers c. diastereomers d. tautomers Que. 11) What is the relationship between D-ribose and D-xylose? CHO CHO І н он н -он нон нон н -он н -он І І CH OH Сн,он...
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...
Homework Problems 8.1 Draw the structural formula for each of the following: a. 5-chloro-4-methyl-2-hexanol b. 2,3-dimethylcyclopentanol c. 5,5-diethyl-1-heptanol d. 2-ethyl-4-isopropylcyclohexanol e. 4-ethylphenol f. 2-nitrophenol g. cyclopropyl methyl ether h. isopropyl propyl ether 8.2 Give the product for the dehydration of each of the following alcohols. CH-CH2-CH3 a. ОН b. ОН C. OH d. 8.3 What product would result from the oxidation of each of the following alcohols? Write the chemical equations. a. 2-butanol b. 2-methyl-2-pentanol c. cyclohexanol d. 3-ethylcyclopentanol Name...
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