Help me with my study guide Draw 3 different isomers with the following characteristics: 1) molecular formula of C3H4Cl2; 2) a ringwith torsional strain. Be sure to indicate stereochemistry if necessary.

The provided answer shows two sets of isomers of the molecular formula C₃H₄Cl₂: 1. Alkene…

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Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 12CTQ: Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth...

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Cyclohexane derivatives exist primarily in the most stable of the available chair conformations. Give the position, axial or equatorial, of each of the three groups shown when the ring is in the most stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq.
Consider 1-bromopropane, CH3CH2CH2Br. (a) Draw a Newman projection for the conformation in which CH3 and -Br are anti (dihedral angle 180°). (b) Draw Newman projections for the conformations in which - CH3 and -Br are gauche (dihedral angles 60° and 300°). (c) Which of these is the lowest energy conformation? (d) Which of these conformations, if any, are related by reflection?
1) Draw the molecule to which the Newman plot below belongs. 2) a) Draw the Newman projection of the most unstable and stable conformations based on the C2-C3 carbons of butane. b) Draw the most stable conformation of cis-1-methyl-3-ethylcyclohexane. 3) Which of the following molecules are structural isomers with each other?
A trisubstituted cyclohexane compound is given in its chair conformation. Draw the corresponding planar (overhead) representation, using wedge-and-dash bonds to indicate the substituent positions. Draw the planar cyclohexane. Clearly show stereochemistry. Select Draw Rings More Era //|の|/ CI H. Br CI F Br
Draw a structural formula of the S configuration of the compound shown below. • Use the wedge /hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • Ifa group is achiral, do not use wedged or hashed bonds on it. CH3 CH3 CH;CHCHCN CH,CH,CH,CHCH,CH, CH2NH2 Draw a structural formula of the RS configuration of the compound shown below. Use the wedge /hash bond tools to indicate stereochemistry where it exists. • Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it. ÇI
Draw a skeletal (line-bond) structure of (R)-2,2,3 trimethylhexane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.
How many isomers (structural, geometric, and stereo) have the formula C5H10, and have "cyclo" in their name? (i.e. they contain a ring) 4 06 07 5
2. How many units of unsaturations does a compound with the formula C25H40Cl4 have? 3. Give the name of this compound, including stereochemistry if relevant: (CH3)3CCH₂CI
Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H₂C CH3 C=C H3C-CH H₂C-CH3 CH3 CH3CH₂ CH3 H3C CH3
Draw a skeletal (bond-line) structure of (R)-2,2,3- trimethylhexane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.
2 1 Group activity: Use molecular model to convert the given 3D perspective structure to Newman projection around C-C bond on the template provided. Fill in the substituent for the most stable conformation in the templates provided. H H OH Br OH CH Y/ 3D of most stable conformation ΕΙ Fischer projection of most stable conformation most stable conformation Use the molecular model of chair conformation of cyclohexane and fill in the substituents in the template provided for chair conformation and complete the Newman projections showing only substituents for given molecules. Circle the chair conformation which is more stable. 1) cis-3-isopropylcyclohexanol 2) trans-3-Isopropylcyclohexaol QO

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Draw 3 different isomers with the following characteristics: 1) molecular formula of C3H4Cl2; 2) a ring with torsional strain. Be sure to indicate stereochemistry if necessary.