raw a chair comformation of cyclohexane with one CH3CH2 group and one CH3 group that fits each description: a). a 1,1-disubstituted cyclohexane with an axial CH3CH2 group b). a cis-1,2-disubstituted cyclohexane with an axial CH3 group c). a trans-1,3-disubstituted cyclohexane with an equatorial CH3 group

raw a chair comformation of cyclohexane with one CH3CH2 group and one CH3 group that fits each description: a). a 1,1-disubstituted cyclohexane with an axial CH3CH2 group b). a cis-1,2-disubstituted cyclohexane with an axial CH3 group c). a trans-1,3-disubstituted cyclohexane with an equatorial CH3 group

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter2: Alkanes And Cycloalkanes

Section2.5: Conformations Of Alkanes And Cycloalkanes

Problem 2.9P: Following is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6. (a)...

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Draw a chair conformation of cyclohexane with one CH3CH2 group and one CH3 group that fits each description. a.a 1,1-disubstituted cyclohexane with an axial CH3CH2 group b. a cis-1,2-disubstituted cyclohexane with an axial CH3 group c. a trans-1,3-disubstituted cyclohexane with an equatorial CH3 group d. a trans-1,4-disubstituted cyclohexane with an equatorial CH3CH2 group.
Draw a chair conformation of cyclohexane with one CH3CH2 group and one CH3 group that fits following description. a trans-1,4-disubstituted cyclohexane with an equatorial CH3CH2 group
Draw a chair conformation of cyclohexane with one CH3CH2 group and one CH3 group that ts each description.a. a 1,1-disubstituted cyclohexane with an axial CH3CH2 groupb. a cis-1,2-disubstituted cyclohexane with an axial CH3 groupc. a trans-1,3-disubstituted cyclohexane with an equatorial CH3 groupd. a trans-1,4-disubstituted cyclohexane with an equatorial CH3CH2 group
Draw a chair conformation of cyclohexane with one CH3CH2 group and one CH3 group that fits following description. a 1,1-disubstituted cyclohexane with an axial CH3CH2 group
Consider the following cyclohexane derivative: *Figure is the screenshot* a. Draw a chair conformation for the cyclohexane derivative above showing equatorial and axial positions at the carbon atoms bearing the substituents. b. Draw the flipped chair conformation showing the axial and equatorial position at the carbon atoms that bear the substituents. Determine which structure is more stable(8a or 8b)? Describe and give your reasons.
For each compound drawn below: a.Label each OH, Br, and CH3 group as axial or equatorial. b.Classify each conformation as cis or trans.c.Translate each structure into a representation with a hexagon for the six-membered ring, and wedges and dashed wedges for groups above and below the ring. d. Draw the second possible chair conformation for each compound.
a)draw the Newman projection b) rotate the back carbon by 60 degree , draw the staggered conformer c) Rotate the back carbon further by 120 degrees, draw the staggered conformer.
Following is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6. (a) Draw hydrogen atoms that are above the plane of the ring on carbons 1 and 2 and below the plane of the ring on carbon 4. (b) Which of these hydrogens are equatorial? Which are axial? (c) Draw the alternative chair conformation. Which hydrogens are equatorial? Which are axial? Which are above the plane of the ring? Which are below it?
On the left is a stereorepresentation of glucose (we discuss the structure and chemistry of glucose in Chapter 25). (a) Convert the stereorepresentation on the left to a planar hexagon representation. (b) Convert the stereorepresentation on the left to a chair conformation. Which substituent groups in the chair conformation are equatorial? Which are axial?
Hello, I was reading an answer from the book Organic Chemistry by Brown et al. The question is 2.51 "Draw alternative chair conformations for each substituted cyclohexane and state which chair is more stable." There are then 4 cyclohexanes (labeled a-d). For the "a" cyclohexane, the substituents are arranged as a combination of axial and equatorial in both chair conformations. However, for the "b," "c," and "d," cyclohexanes one chair has only equatorial substituents, and the other chair has only axial substituents. Why is the "a" chair conformation different? https://www.bartleby.com/solution-answer/chapter-2-problem-251p-organic-chemistry-8th-edition/9781305580350/draw-alternative-chair-conformations-for-each-substituted-cyclohexane-and-state-which-chair-is-more/4532cd91-c341-11e9-8385-02ee952b546e
Draw a three-dimensional structure for each compound, and star all asymmetric carbon atoms. Draw the mirror image for each structure, and state whether you have drawn a pair of enantiomers or just the same molecule twice. Build molecular models of any of these examples that seem difficult to you. chlorocyclohexane
Consider the tricyclic structure B. (a) Label each substituent on the rings as axial or equatorial. (b) Draw B using chair conformations for each six-membered ring. (c) Label the atoms on the ring fusions (the carbons that join each set of two rings together) as cis or trans to each other.