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Free response 1. 2 points Two molecules that have the same connectivity and are non other...
es of each 1. 2 points Two molecules that have the same connectivity and Es that...
es of each 1. 2 points Two molecules that have the same connectivity and Es that have the same connectivity and are nonsunerimposable mirror images of eac other are called 2. 4 points for the following molecule. label each stereocenter with an asterisk .am configurational isomers. tereocenter with an asterisk (*), and then draw all possible 3. 4 points Which of the following alkenes is more stable? Explain. 4. 2 points A molecule has two rings, three double bonds, and...
1. Chirality (6pts, 2EA) Arethe following carbons indicated by the arrow stereogenic-a chiral carbon center). Write...
1. Chirality (6pts, 2EA) Arethe following carbons indicated by the arrow stereogenic-a chiral carbon center). Write yes or DATE: 1104.19 No and explain? Н Нс. Br H Hас" Et 2 CONFIGURATIONS (2PTS, IEA) Assign stereoisomer configuration using R or S nomenclature (NOTE: priorities have been preassigned using Cahn-Ingold-Prelog convention) 3. Multiple Choice-Definition (1pt): Define enantiomers: (Circle the correct choice) Molecules with same molecular formula, and connectivity, but differ in 3-dimenisonal space a. b. Molecules with same molecular formula, and connectivity,...
Constitutional Isomers-same MF, diff. connectivity Enantiomers-stereoisomers, mirror image, not superimposable Diastereomers-stereoisomers, not mirror image Same-same MF,...
Constitutional Isomers-same MF, diff. connectivity Enantiomers-stereoisomers, mirror image, not superimposable Diastereomers-stereoisomers, not mirror image Same-same MF, same connectivity, same spatial arrangement Different-different MF (12 points) 8. In the boxes below, give the relationship between the pairs of molecules. Possible terms are shown at right. Each term may be used more than once and some terms may not be used at all. Cl Br CHy CHs CH and and CHS Cl H Br н CH3 CHs H CHs CHs and CHg...
1. Construct a model consisting of a tetrahedral carbon center with four different component atoms attached:...
1. Construct a model consisting of a tetrahedral carbon center with four different component atoms attached: red, white, blue, green; each color represents a different group or atom attached to carbon. Does this model have a plane of symmetry (1a)? A plane of symmetry can be described as a cutting plane-a plane that when passed through a model or object divides it into two equivalent halves; the elements on one side of the plane are the exact reflection of the...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
Organic Chemistry Organic Chemistry Organic Chemistry Problems Stereochemistry This one has more me thol graps allocted...
Organic Chemistry Organic Chemistry Organic Chemistry Problems Stereochemistry This one has more me thol graps allocted so it toves ponty between these 2 deeres. The curcled one has a Tripe bord so it acts as of it's attached to 3 moe Carbors º-c=o- Problem 3: Clearly indicate of the following molecules are chiral or achiral. If a molecules chiral assign priority numbers to each group that surround the chiral atom. но 0 OH OH Cheral chiral CH3 Chinal Problem 4:...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
This is the best copy I have. This is exactly what I received Model 3: Representations...
This is the best copy I have. This is exactly what I
received
Model 3: Representations of methylcyclobutane H Skeletal Ball-and-stick Wedee and Wedge and dash Perspective ("stick") Cash with explicit hydrogens Model 4: 1.2-dimethylcyclobutane, shown with ring carbons numbered 1-4 (b) LACH 2CH SCH Name (9) Are the molecules in boxes (a) and (b) of Model 4 constitutional womers of each other? Explain 10. Pher than bonds to cartons within the ring, what we aroups are bonded to the...
What is the relationship between these two molecules? a) They have the same configuration b) They...
What is the relationship between these two molecules?
a) They have the same configuration
b) They are cis-trans isomers
c) They are enantiomers of each other
d) They are diastereomers of each other
e) None of the above
CH3 H-C-X H-C-Y H-C-Y CH3
1.A. Place an asterisk (*) next to each stereocenter of these four compounds. 1.3. Bubble in...
1.A. Place an asterisk (*) next to each stereocenter of these four compounds. 1.3. Bubble in if the compound is chiral or achiral. 1.C. Determine the stereochemical relationship between each possible pair. Br Br Br Br A B D chiral O achiral OO chiral achiral с Ochiral achiral 8 chiral achiral A and B: 000 identical enantiomers diastereomers none of these A and C: ооо identical enantiomers O diastereomers none of these A and D: оооооо O identical enantiomers diastereomers...
es of each 1. 2 points Two molecules that have the same connectivity and Es that have the same connectivity and are nonsunerimposable mirror images of eac other are called 2. 4 points for the following molecule. label each stereocenter with an asterisk .am configurational isomers. tereocenter with an asterisk (*), and then draw all possible 3. 4 points Which of the following alkenes is more stable? Explain. 4. 2 points A molecule has two rings, three double bonds, and...
1. Chirality (6pts, 2EA) Arethe following carbons indicated by the arrow stereogenic-a chiral carbon center). Write yes or DATE: 1104.19 No and explain? Н Нс. Br H Hас" Et 2 CONFIGURATIONS (2PTS, IEA) Assign stereoisomer configuration using R or S nomenclature (NOTE: priorities have been preassigned using Cahn-Ingold-Prelog convention) 3. Multiple Choice-Definition (1pt): Define enantiomers: (Circle the correct choice) Molecules with same molecular formula, and connectivity, but differ in 3-dimenisonal space a. b. Molecules with same molecular formula, and connectivity,...
Constitutional Isomers-same MF, diff. connectivity Enantiomers-stereoisomers, mirror image, not superimposable Diastereomers-stereoisomers, not mirror image Same-same MF, same connectivity, same spatial arrangement Different-different MF (12 points) 8. In the boxes below, give the relationship between the pairs of molecules. Possible terms are shown at right. Each term may be used more than once and some terms may not be used at all. Cl Br CHy CHs CH and and CHS Cl H Br н CH3 CHs H CHs CHs and CHg...
1. Construct a model consisting of a tetrahedral carbon center with four different component atoms attached: red, white, blue, green; each color represents a different group or atom attached to carbon. Does this model have a plane of symmetry (1a)? A plane of symmetry can be described as a cutting plane-a plane that when passed through a model or object divides it into two equivalent halves; the elements on one side of the plane are the exact reflection of the...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
Organic Chemistry Organic Chemistry Organic Chemistry Problems Stereochemistry This one has more me thol graps allocted so it toves ponty between these 2 deeres. The curcled one has a Tripe bord so it acts as of it's attached to 3 moe Carbors º-c=o- Problem 3: Clearly indicate of the following molecules are chiral or achiral. If a molecules chiral assign priority numbers to each group that surround the chiral atom. но 0 OH OH Cheral chiral CH3 Chinal Problem 4:...
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
This is the best copy I have. This is exactly what I
received
Model 3: Representations of methylcyclobutane H Skeletal Ball-and-stick Wedee and Wedge and dash Perspective ("stick") Cash with explicit hydrogens Model 4: 1.2-dimethylcyclobutane, shown with ring carbons numbered 1-4 (b) LACH 2CH SCH Name (9) Are the molecules in boxes (a) and (b) of Model 4 constitutional womers of each other? Explain 10. Pher than bonds to cartons within the ring, what we aroups are bonded to the...
What is the relationship between these two molecules?
a) They have the same configuration
b) They are cis-trans isomers
c) They are enantiomers of each other
d) They are diastereomers of each other
e) None of the above
CH3 H-C-X H-C-Y H-C-Y CH3
1.A. Place an asterisk (*) next to each stereocenter of these four compounds. 1.3. Bubble in if the compound is chiral or achiral. 1.C. Determine the stereochemical relationship between each possible pair. Br Br Br Br A B D chiral O achiral OO chiral achiral с Ochiral achiral 8 chiral achiral A and B: 000 identical enantiomers diastereomers none of these A and C: ооо identical enantiomers O diastereomers none of these A and D: оооооо O identical enantiomers diastereomers...
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