Draw all possible stereoisomers for each of the following.(a). 2- chloro-3-hexanol. (b). 2-bromo-4- chlorohexane . (c)...
Draw all possible stereoisomers for each of the following.(a). 2- chloro-3-hexanol. (b). 2-bromo-4- chlorohexane . (c) 2,3,-diachloro pentane. (d). 1,3-diabromopentane.(2) .Draw the stereoisomers of 2-methylcyclohexane.
Homework Answers
Stereoisomers
having same molecular formula but different structural formula.
Add Answer to:
Draw all possible stereoisomers for each of the following.(a).
2- chloro-3-hexanol. (b). 2-bromo-4- chlorohexane . (c)...
For 2-chloro-3-hexanol: Draw the structure of all the possible stereoisomers with Fischer Projection and Perspective Formulas...
For 2-chloro-3-hexanol: Draw the structure of all the possible stereoisomers with Fischer Projection and Perspective Formulas showing both eclipsed and staggered conformations). 2) Assign the configuration of all chiral centers with R or S. (3) Give the complete IUPAC name for each stereoisomers. (4) Indicate the relationship among the structures, indicating which are the threo or erythro enantiomer, and diastereoisomer pairs.
Which is the best SN2 substrate? a.2-chloro-2-methylhexane b.2-chlorohexane c.1-chlorohexane Which substrate will react fastest via an...
Which is the best SN2 substrate? a.2-chloro-2-methylhexane b.2-chlorohexane c.1-chlorohexane Which substrate will react fastest via an SN1 mechanism? a.1-bromo-2-methylcyclohexane b.1-bromo-1-methylcyclohexane c.bromocyclohexane Which of the following is capable of a rearrangement once the leaving group leaves? a.1-bromo-4-methylcyclohexane b.1-bromo-1-methylcyclohexane c.1-bromo-2-methylcyclohexane d.bromocyclohexane
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene...
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene 1-ethyl-3-methyl-2-propylcyclopentane 2-Keto-1,3-propandioic acid
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
2) a) Consider 2-bromo-3-chlorobutane. How many stereoisomers are possible for this compound? Draw all stereoisomers, label...
2) a) Consider 2-bromo-3-chlorobutane. How many stereoisomers are possible for this compound? Draw all stereoisomers, label each stereocenter with the appropriate R/S designation to show handedness, and indicate the relationship (enantiomers or diastereomers) between every possible pairing of compounds. Name each compound according to IUPAC nomenclature, using appropriate R/S designation to show handedness. b) Repeat this exercise for 2,3-Butanediol. What is different about this compound relative to the first example? What word describes the unique stereoisomer? c) Which of the...
2. Starting with ethyne and any necessary reagents to synthesize enantiomers of (3S,4R)-4-bromo-3-hexanol and (3R,4S)-4-bromo-3-hexanol. H5C2...
2. Starting with ethyne and any necessary reagents to synthesize enantiomers of (3S,4R)-4-bromo-3-hexanol and (3R,4S)-4-bromo-3-hexanol. H5C2 H5C2 H- OH HO -H Several steps HCECH H- -Br Br -H C2H5 C₂H5 3. Write mechanism for the following reaction and draw the possible structures for Cand D. NaBr/H,SO + + C + D Br Br
Draw the most stable conformation for; a. trans-1-chloro-3-methylcyclohexane b. cis-1-ethyl-2-isopropylcyclohexane c. trans-1-bromo-4-ethylcyclohexane d. cis-2-bromo-1-methylcycclohexane Sppecifically, show...
Draw the most stable conformation for; a. trans-1-chloro-3-methylcyclohexane b. cis-1-ethyl-2-isopropylcyclohexane c. trans-1-bromo-4-ethylcyclohexane d. cis-2-bromo-1-methylcycclohexane Sppecifically, show the ring flipping and calculate the strain using the table given in the power point slides.
Draw all stereoisomers associated with 2-Bromo-3-methypentane. Draw the Fischer projections for all stereoisomers associated with 2-Bromo-3-methypentane....
Draw all stereoisomers associated with 2-Bromo-3-methypentane.
Draw the Fischer projections for all stereoisomers associated with
2-Bromo-3-methypentane. Clearly label all stereoisomers as either
enantiomers, diastereomers, or meso. Place the lowest priority
groups in two vertical positions in final display. SHOW ALL WORK
CLEARLY. Thank you!
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
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...
For 2-chloro-3-hexanol: Draw the structure of all the possible stereoisomers with Fischer Projection and Perspective Formulas showing both eclipsed and staggered conformations). 2) Assign the configuration of all chiral centers with R or S. (3) Give the complete IUPAC name for each stereoisomers. (4) Indicate the relationship among the structures, indicating which are the threo or erythro enantiomer, and diastereoisomer pairs.
3. Write the structure of following organic compounds (15 points) 3-Chloro-5,7-dimethyl-4-cyclopropyl-2-octene 2-amino-3-methyl-2-nitro-butanal 2-Bromo-4-nitro-3-hexanol Aminomethanamide 2-Chloro-3-methyl-1-cyclopentanone 2-bromo-3-methyl-2-pentene 1-ethyl-3-methyl-2-propylcyclopentane 2-Keto-1,3-propandioic acid
Draw structures for the following compounds. a. 2-chloro-1,3-cyclopentadiene b. 2-bromo-5-nitroaniline c. 2-chloro-5-fluoro-3-octyne
2) a) Consider 2-bromo-3-chlorobutane. How many stereoisomers are possible for this compound? Draw all stereoisomers, label each stereocenter with the appropriate R/S designation to show handedness, and indicate the relationship (enantiomers or diastereomers) between every possible pairing of compounds. Name each compound according to IUPAC nomenclature, using appropriate R/S designation to show handedness. b) Repeat this exercise for 2,3-Butanediol. What is different about this compound relative to the first example? What word describes the unique stereoisomer? c) Which of the...
2. Starting with ethyne and any necessary reagents to synthesize enantiomers of (3S,4R)-4-bromo-3-hexanol and (3R,4S)-4-bromo-3-hexanol. H5C2 H5C2 H- OH HO -H Several steps HCECH H- -Br Br -H C2H5 C₂H5 3. Write mechanism for the following reaction and draw the possible structures for Cand D. NaBr/H,SO + + C + D Br Br
Draw the most stable conformation for; a. trans-1-chloro-3-methylcyclohexane b. cis-1-ethyl-2-isopropylcyclohexane c. trans-1-bromo-4-ethylcyclohexane d. cis-2-bromo-1-methylcycclohexane Sppecifically, show the ring flipping and calculate the strain using the table given in the power point slides.
Draw all stereoisomers associated with 2-Bromo-3-methypentane.
Draw the Fischer projections for all stereoisomers associated with
2-Bromo-3-methypentane. Clearly label all stereoisomers as either
enantiomers, diastereomers, or meso. Place the lowest priority
groups in two vertical positions in final display. SHOW ALL WORK
CLEARLY. Thank you!
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...
Most questions answered within 3 hours.
-
Fiscal policy is the deliberate manipulation of taxes and
government spending to alter GDP, employment, inflation...
asked 38 minutes ago -
evaluating an expression using only one digit and + and - as
operators ....3+5-1+7-5+8
-----------------------
stack...
asked 38 minutes ago -
Two concentric current loops lie in the same plane. The smaller
loop has a radius of...
asked 1 hour ago -
1)Which of the following is an
important difference between qualified and nonqualified retirement
plans?
a. Qualified...
asked 1 hour ago -
What's the streaming business's problem on the
horizon?
asked 2 hours ago -
I need help with writing the conclusion for this online lab
report
Abstract
By testing the...
asked 2 hours ago -
For the reaction 1N2+3H2-----> 2NH3, would the reaction rate
trend be: delta[NH3]/ delta t = -2...
asked 3 hours ago -
Within your current/past organization, identify a problem/issue
and format a design to address same. You may...
asked 2 hours ago -
A sock stuck to the side of a clothes-dryer barrel has a
centripetal acceleration of 24...
asked 3 hours ago -
A perfect gas undergoes an isentropic process such that its
volume doubles. If the ratio of...
asked 4 hours ago -
list the elements in groups 3A to 6A in the same order as in the
periodic...
asked 4 hours ago -
Estimating effect size. Peng and Chen (2014)
evaluated effect size estimates for various tests. In their...
asked 4 hours ago