A pair of theoretical enantiomers is named below. For each stereoisomer, draw the structure. Be sure...
A pair of theoretical enantiomers is named below. For each stereoisomer, draw the structure. Be sure to specify the stereochemistry via wedge-and-dash bonds
Homework Answers
This problem is based on the concept of enantiomers.
Isomers that have same molecular formula but different arrangement of atoms in space or different bonding between atoms in such a way that their absolute configuration is exactly opposite are called Enantiomers.
Enantiomers can be determined by using their structure determination and absolute configuration. Enantiomers are non-superimposable mirror image of each other.
The name of first compound is (S)-5,5-dibromo-3-flouro-2-methyl-3-hexanol.
Structure of the compound is given below:
The name of first compound is (R)-5,5-dibromo-3-flouro-2-methyl-3-hexanol.
Structure of the compound is given below:
Structure of (S)-5,5-dibromo-3-flouro-2-methyl-3-hexanol is as follows:
Structure of (R)-5,5-dibromo-3-flouro-2-methyl-3-hexanol is as follows:
if you have any doubts about
the answer please mention in the comments please do rate the answer
.
Add Answer to:
A pair of theoretical enantiomers is named below. For each stereoisomer, draw the structure. Be sure...
Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Use wedge-and-dash bonds for the substituent groups, and be sure that...
Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Use wedge-and-dash bonds for the substituent groups, and be sure that they are drawn on the outside of the ring, adjacent to each other. The skeletal structure of one molecule is included to indicate the proper format; modify the X\'s on the given structure to create the first stereoisomer..
2. Analyze each pair of compounds below. Identify which class of isomers each pair of structures...
2. Analyze each pair of compounds below. Identify which class of isomers each pair of structures represent. Your choices are: (i) constitutional, (ii) conformational, (iii) enantiomers, or (iv) diastereomers. Only one label for each pair should be used. For each case show work (drawings, (R)/(S), rotation of bonds, chair-flips, etc) which led you to each answer for the pairs below. Any differences of answers between you and your peers can be discussed and corrected as needed. OH H, H носно...
need help with #2 Enantiomeric pairs: Diastereomeric pairs: Identical molecules: 2. For the structure given below,...
need help with #2
Enantiomeric pairs: Diastereomeric pairs: Identical molecules: 2. For the structure given below, the name of a specific stereoisomer is given. Show the stereochemistry of the named stereoisomer using a perspective (dash & wedge) structure, a staggered Newman projection and a Fischer projection. (3 pts) он о Y O H (2R,3R)-3-hydroxy-2-nitropentanoic acid NO 7 change ( 3. Decide whether each of the following pairs of structures represent enantiomers, diastereomers, or identical molecules (6 pts) ame one crates
For the stereoisomers below, use the R/S configuration given in the compound name to finish drawing the structure by...
For the stereoisomers below, use the R/S configuration given in
the compound name to finish drawing the structure by connecting the
appropriate groups. Be sure to specify the stereochemistry via
wedge-and-dash bonds. If needed, you may restore a module to its
orignal state by clicking on the module and then clicking on the
red over-under arrows.
Draw one product structure for the following Diels–Alder reaction. For ONLY the chirality...
Draw one product structure for the following Diels–Alder
reaction. For ONLY the chirality centers with D and C(=O)H groups,
specify the stereochemistry via wedge-and-dash bonds. (D is
deuterium, an isotope of hydrogen. Include it in your drawing by
either double clicking on an atom and typing \"d\" or by choosing D
in the bottom row of the atoms menu.)
3B) Draw the constitutional isomers of trimethylcyclopropane as skeletal structures. 3C) For each constitutional isomer you...
3B) Draw the constitutional isomers of trimethylcyclopropane as
skeletal structures.
3C) For each constitutional isomer you drew in part (a), draw
any stereoisomers of that structure, explicitly showing
stereochemistry with dash/wedge bonds. Use skeletal structures.
2. This molecule has a ring strain of 70 kl/mol. Circle which type of strain is most important, and explain why you circledit: Angle torsional steric 3. Only one stereoisomer of this compound is stable - draw the relative stereochemistry at the ring Junction with...
Draw one product structure for the following Diels-Alder reaction. For ONLY the chirality centers with D...
Draw one product structure for the following Diels-Alder reaction. For ONLY the chirality centers with D and C(=0)H groups, specify the stereochemistry via wedge-and-dash bonds. (D is deuterium, an isotope of hydrogen. Include it in your drawing by either double clicking on an atom and typing "d" or by choosing D in the bottom row of the atoms menu.)
4. (18pts) Consider the bond-line structure below. (a) How many stereoisomers are predicted for this compound?...
4. (18pts) Consider the bond-line structure below. (a) How many stereoisomers are predicted for this compound? Why are the actual number of stereoisomers for this compound less than the predicted amount? (b) Draw the stereoisomers, clearly showing stereochemistry with dash/wedge notation. (c) Label each pair of stereoisomers as either enantiomers or diastereomers and identify which pair(s) are optically inactive as a 50/50 mixture. XX
The structure of a chiral isomer is given below. Draw the mirror image isomer. The structure...
The structure of a chiral
isomer is given below. Draw the mirror image isomer.
The structure of a chiral isomer is given below. Draw the mirror image isomer. Use wedge-and-dash bonds for the substituent groups, and be sure that the bonds convey tetrahedral geometry.
Question 8.38 This reaction is incorrect as written. In the box below draw the structure of...
Question 8.38 This reaction is incorrect as written. In the box below draw the structure of the correct product. If a reaction forms a racemic mixture draw both of the stereoisomers. Use wedge/dash bonds as necessary to indicate stereochemistry.
2. Analyze each pair of compounds below. Identify which class of isomers each pair of structures represent. Your choices are: (i) constitutional, (ii) conformational, (iii) enantiomers, or (iv) diastereomers. Only one label for each pair should be used. For each case show work (drawings, (R)/(S), rotation of bonds, chair-flips, etc) which led you to each answer for the pairs below. Any differences of answers between you and your peers can be discussed and corrected as needed. OH H, H носно...
need help with #2
Enantiomeric pairs: Diastereomeric pairs: Identical molecules: 2. For the structure given below, the name of a specific stereoisomer is given. Show the stereochemistry of the named stereoisomer using a perspective (dash & wedge) structure, a staggered Newman projection and a Fischer projection. (3 pts) он о Y O H (2R,3R)-3-hydroxy-2-nitropentanoic acid NO 7 change ( 3. Decide whether each of the following pairs of structures represent enantiomers, diastereomers, or identical molecules (6 pts) ame one crates
For the stereoisomers below, use the R/S configuration given in
the compound name to finish drawing the structure by connecting the
appropriate groups. Be sure to specify the stereochemistry via
wedge-and-dash bonds. If needed, you may restore a module to its
orignal state by clicking on the module and then clicking on the
red over-under arrows.
3B) Draw the constitutional isomers of trimethylcyclopropane as
skeletal structures.
3C) For each constitutional isomer you drew in part (a), draw
any stereoisomers of that structure, explicitly showing
stereochemistry with dash/wedge bonds. Use skeletal structures.
2. This molecule has a ring strain of 70 kl/mol. Circle which type of strain is most important, and explain why you circledit: Angle torsional steric 3. Only one stereoisomer of this compound is stable - draw the relative stereochemistry at the ring Junction with...
Draw one product structure for the following Diels-Alder reaction. For ONLY the chirality centers with D and C(=0)H groups, specify the stereochemistry via wedge-and-dash bonds. (D is deuterium, an isotope of hydrogen. Include it in your drawing by either double clicking on an atom and typing "d" or by choosing D in the bottom row of the atoms menu.)
4. (18pts) Consider the bond-line structure below. (a) How many stereoisomers are predicted for this compound? Why are the actual number of stereoisomers for this compound less than the predicted amount? (b) Draw the stereoisomers, clearly showing stereochemistry with dash/wedge notation. (c) Label each pair of stereoisomers as either enantiomers or diastereomers and identify which pair(s) are optically inactive as a 50/50 mixture. XX
The structure of a chiral
isomer is given below. Draw the mirror image isomer.
The structure of a chiral isomer is given below. Draw the mirror image isomer. Use wedge-and-dash bonds for the substituent groups, and be sure that the bonds convey tetrahedral geometry.
Question 8.38 This reaction is incorrect as written. In the box below draw the structure of the correct product. If a reaction forms a racemic mixture draw both of the stereoisomers. Use wedge/dash bonds as necessary to indicate stereochemistry.
Most questions answered within 3 hours.
-
when 2053 j of heat is added to 46.3 g of hexane C6H14 the
temperature increases...
asked 15 minutes ago -
I need new and unique answers, please. (Use your own words,
don't copy and paste), Please...
asked 18 minutes ago -
MCL 445.111 et seq. deals with Home Solicitation Sales.
MCL stands for Michigan Compiled Laws which...
asked 9 minutes ago -
Which of the following items may not create an NOL?
a.
sole proprietorship loss
b.
personal...
asked 14 minutes ago -
A hypothetical solution forms between a solid and a liquid. The
values of the thermodynamic quantities...
asked 12 minutes ago -
a)An ideal heat pump is being considered for use in heating an
environment with a temperature...
asked 15 minutes ago -
.
Convert the following pairs of voltage and current waveforms to
phasor form. Each pair of...
asked 17 minutes ago -
A 6.5 cm diameter ball has a terminal speed of 22 m/s. What is
the ball's...
asked 31 minutes ago -
Name two areas of the human body with the highest concentration
of lymph nodes and speculate...
asked 34 minutes ago -
Angel Corporation has $10,000,000 of
8.0% 25 year bonds dated May 1, 2018 with interest payable...
asked 1 hour ago -
7.
________ involves individuals trading goods they already have or
providing services in exchange for something...
asked 1 hour ago -
Share your research problem. What databases did you search as
you gathered evidence to support your...
asked 1 hour ago