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3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules...
3. Cyclic compounds The presence of the ring in all but very large ring cyclic molecules prevents full rotation of the ring atoms. For this reason, stereoisomerism may also occur in cyclic molecules. a) Prepare a model of cyclohexane, CH12. Draw the condensed formula b) Build a model of methylcyclohexane (C;H2a) by replacing one of the hydrogens of cyclohexane with a methyl group. Draw the skeletal formula for methylcyclohexane. c) How many different isomers exist for methylcyclohexane (C-Ha)? d) Start...
A. Enantiomers: Certain substances have the unique property of rotating the plane of plane-polarized light. Such light rotation is detectable with the aid of a polarimeter. In order for a molecule to be optically active it must be chiral. Chiral objects lack a plane of symmetry and are non-superimposable on their mirror images. A sp?- hybridized carbon atom can fulfill these requirements if all four of its substituents are different. 1. Methane a) Prepare a methane molecule and then substitute...
TU c) Start with the model of propene built in 3a), substituting different hydrogen atoms of propene with a methyl group to form isomers of butene, CaHg. How many different isomers exist for butene (C4Hg)? Prepare models and draw the Lewis structures for each of the isomers. d) Two of isomers of butene comprise a pair of stereoisomers. Draw the skeletal structures and include IUPAC names for the cis and trans isomers. Recall in the cis isomer both methyl groups...
Week 1l-seed somers.cf G Sotes of Teile Week 11-Stereoisomers.pdt X file:///C/Users/hp/Downloads/Week 11 Stereoisomers.pdf Automatic Zoom aj Prepare a mouer or cyclonexante, C6H12. Draw the condensed mommula. b) Build a model of methylcyclohexane (C7H14) by replacing one of the hydrogens of cyclohexane with a methyl group. Draw the skeletal formula for methylcyclohexane. 2 c) How many different isomers exist for methylcyclohexane (C7H14)? d) Start with the model of methylcyclohexane built in 4b), substitute different hydrogen atoms on the carbon atoms adjacent...
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4. Enantiomers.- THIS FOLLOWING EXERCISES ON PAGES 6 AND 7 ARE TO BE DONE AS A GROUP WITH THE LAB INSTRUCTOR!!!! a) Construct a model consisting of a tetrahedral carbon center with four different atoms attached - use white, green, orange and violet balls. Each color represents a different group or atom attached to the central carbon. Does this model have a plane of symmetry? Note 1: a plane of symmetry can be described as a cutting...
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PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of 2,3-butanediol as you can. First, attach two carbons with a single bond. To each carbon add one carbon, one hydrogen, and one oxygen. To complete the structure, Ti the remaining hydrogen atoms. Remember, a model is not different if it is completely superimposable on one already constructed! 13. How many stereochemically different models are possible for 2,3-butanediol? 14. What characteristic does one of these...
CHCH(OH)-CH(OH)-CH3 PART 3: 23-BUTANEDIOL Build as many models of 2.3-butanediol as you can. First, attach two carbons with a single bond To each carbon add one carbon, one hydrogen, and one oxygen. To complete the structure. fill in the remaining hydrogen atoms. Remember, a model is not different if it is completelv superimposable on one already constructed! 13. How many stereochemically different models are possible for 2.3-butanediol? 14. What characteristic does one of these models have that makes it different?...
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7D. Complete the following Fischer projections for all 4 of your models and assign Rand S to all chiral carbons. Label the pairs of enantiomers and the pairs of diastereomers. COOH COOH COOH COOH НО- -Н Н- СН3 COOH Союн COOH соон 7A. Complete the following Fischer projections for the three tartaric acid isomers. Label the pair of enantiomers, a pair of diastereomers, and the meso isomer. Assign R or S designations to all chiral carbons. COOH...
rojection Formulas for each model in #16 (again orient the carbon chain up and down). Are the mirror images "superimposable?" Interchange any two of the groups located at one of the chiral centers on one of the models in # 1 6. What is the stereochemical relationship of the resulting structure with the one that used to be its mirror image? Will this 'new' model be "optically active?" Why or why not? 18. PART 4:2,3-DICHLOROPENTANE CH, CH(C)-CHC)-CH2CH Build a model...
Circle all the molecules that have an internal plane of symmetry. Note: rotation around a C-C bond may be required to see a plane of symmetry (0.4 pts) HCI OH OH H Quinox is a P-stereogenic bisphosphine ligand. Determine the (RS) configurations of the phosphorus atoms, draw the mirror image of the compound, and label the compound as chiral or achiral. (0.5 pts) Chiral or Achiral? If one of the two chiral centers in a molecule has the R-configuration and...