1. Using a Model set Build a model for the following compound [CHBRIF]2. Build another model of the mirror image of your first molecule.3. Place the two models next to each other and take a picture which shows thedifferences between the two models.4. Determine the absolute stereochemistry R or S for the two models.5. Write or type a paragraph to Discuss the stereochemical relationshipbetween the two models of CHBгCIF. You must provide an explanation foryour conclusions also provide a description for the colors used to represent

1. The molecule CHBrIF can be modelled as the following image. In the given image, the red atom…

Answered: 1. Using a Model set Build a model for…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 1CTQ

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Draw a stereoisomer of cis-1,2-dimethylcyclohexane. (Note that the question asks for a different stereoisomer of the named compound and not the named compound itself.) • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • In cases where there is more than one answer, just draw one. Y TAYY n[] ChemDoodle
5. Construct models of all the stereoisomers of 1-bromopropene. Draw the line structure of your models. Are these molecules isomers? If they are isomers to what specific category do they belong? Assign E or Z descriptors to each compound, if appropriate. 6. Construct a model of dibromochloromethane and draw the perspective structure. How many planes of symmetry does this molecule possess? Construct the mirror image of your model. Are the two models superimposable? Classify or describe the relationship between these two mirror images, and assign R or S descriptors, if appropriate.
Sight along the C2-Cl bond of 2-methylpropane (isobutane). a. Draw a Newman projection of the most stable conformation. b. Draw a Newman projection of the least stable conformation. c. Make a graph of energy versus angle of rotation around the C2-Cl bond. d. Assign relative values to the maxima and minima in your graph, given that an H↔H eclipsing interaction costs 0 kJ/mol and an H↔CH3 eclipsing interaction costs 6.0 kJ/mol.
Stereoisomers are isomers that differ in spatial arrangement of atoms, rather than connectivity of atoms. Stereoisomers have different properties, especially in biological systems. Which is the stereochemical relationship between this pair of molecules? OH "OH 8p OH OH ...||| 4 A) enantiomers B) diastereomers C) identical compounds D) constitutional isomers E) Not isomers
ぐ=m, Part 4: Cycloalkanes and Stereochemistry. assignment. Br Br Br ...|H ...H ... H ..iBr H. Br Br .... ICH3 H. 18. For rings that an the and label each atom as R or S. Some rings will not have an R or S
2 2. Draw all possible conformations for 1,1,2-tribromopropane. Label all unfavc interactions. Which conformation is most stable? Explain. TI
In this question, you will draw all the constitutional isomers of CH4Br₂. This compound has an IHD of 1, which means it will either have one ring or one double bond. For this question, do not consider stereoisomers.
Pls help ASAP. Pls circle the final answer
Draw the optically inactive stereoisomer(s) of 1,2-dimethylcyclohexane. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with + signs from the drop-down menu. ● ? ChemDoodle n [ ]#
Connections to biology 6. Idose is a monosaccharide (i.e. sugar) molecule. The structure shown on the left below represents one form of idose in a six-membered ring. Draw the two chair conformations of this molecule using the templates. Note that the positions of carbon 1 are marked in all structures. OH HO 2 OH LO 1, OH OH OH
HO CH3 a. Label with asterisks (*) all of the stereocentres in the molecule shown above. b. How many stereoisomers are possible? c. Draw the structures of one pair of enantiomers for the above molecule. (Hint: You should draw two structures using wedge and dashed wedge bonds.)
||| O STEREOCHEMISTRY Identifying the enantiomer of a simple organic molecule ander Coen Stractare in the table that is an Chianciom CHICER the tabl H CI ****** Br Explanation ay Molecule 1 BL CI Br H 0 Molecule 4 ****** H Br CI Onone of the above Check 1019 Molecule 2 Br H Cl 0 Molecule 5 Br ""H CI OCT 4 WITC Molecule 3 HO CI tv ♫ ***** Molecule 6 Br H hone *** CI H Br Tent ore, CHECK the home X OF CHIC 5 0/5 DOX Under Olivia Ⓒ2023 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | A TAO

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