Draw the Newman projections for the most and least stable conformations and indicate what strain(s) the least stable conformation has. Look in the direction of arrow. This is the structural formula for (R)-3-Fluoro-3-methyl-2-butanol, an organic compound. ### Explanation:- **Carbon Backbone**: The structure includes a four-carbon chain. The main chain appears in a zigzag line format, which is typical for organic line structures.- **Functional Groups**: - The hydroxyl group (OH) is attached to the second carbon in the chain. - There is a fluorine atom (F) attached to the third carbon in the chain.- **Stereochemistry**: - The structure includes wedge-and-dash notation to indicate stereochemistry. - The solid wedge (pointing towards the viewer) indicates that the group (a CH3 group) is coming out of the plane of the page. - The dashed line (pointing away from the viewer) indicates that the fluorine atom is going into the plane of the page. - This configuration suggests that it is the R-enantiomer of 3-fluoro-3-methyl-2-butanol.- **Branches**: - There is a methyl group (CH3) attached to the third carbon, supporting the complexity of the structure.This compound can have various applications and relevance in organic chemistry, studying enantiomers, and understanding stereochemistry.

Answered: Image /qna-images/answer/9498e974-1181-408b-a1c6-fd28b0926576.jpg

Answered: ОН | bartleby

Science

Chemistry

ОН

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Related questions

Q: Convert the following to Newman projections looking down the indicated bond RIGHT to LEFT RIGHT to…

Q: Specify the types of strain that destabilize the conformer shown below. Hint: All bonds not…

A: Given is structure of organic compound.Name of given compund is,2-methylbutane

Q: In the most stable chair conformation of the molecule shown, which terms correctly describe the…

A: Alkanes are organic compounds that contain single bonds between carbon atoms in a compound.

Q: Draw the structure below as a Newman projection looking down the indicated bond in the conformation…

A: The Newman projection represents the dihedral angles of different conformations of a molecule. In…

Q: Problem: Answer the following questions about the 2-ethyl-4-isopropyl-1- methylcylcohexane…

A: The planar structure of the cyclohexane molecule is highly unstable due to the high angle strain.…

Q: In box C, draw the Newman projection corresponding to the wedge/slash drawing below with the…

A: A question based on organic chemistry, which is to be accomplished.

Q: Draw both chair conformers of the following substituted cyclohexanes. Identify all significant…

A: Given molecules are two cyclohexane derivatives.

Q: For the molecule shown below, draw both chair conformations and circle which is the lower energy…

A: The given molecule is (1S,2S,4S)-1,2,4-trifluorocyclohexane. It contains three fluorine group…

Q: a) i) Draw the Newman projections for the conformations of ethane (staggered and eclipsed)…

A: In this question we have to draw the Newman projection of Ethane in compare their stability that is…

Q: Explain well with perfect type Answer.

A: The question is based on the concept of conformation of cyclohexane. We need to identify the most…

Q: Compare the following conformers of butan-2-ol. Match each conformer to their corresponding relative…

A: As the bulkyl group near to each other repulsion will increase energy will also increase 2 molecule…

Q: Answer the questions about the molecule shown here. H Br This molecule is shown in its most stable…

A: In Newman projection the stable conformation has bulkier group on front and back carbon at…

Q: Draw both chair conformers of ethylcyclohexane. Identify which is lower in energy.

Q: ОН

A: Newman projection - One front carbon indicated by dot and its adjacent back carbon is indicated by…

Q: 3.39 The following are representations of two forms of glucose. The six-membered ring is known to…

A: Conformational isomers are a type of stereoisomer where one isomer is converted to another isomer.…

Q: Please answer the two following questions using the molecule shown below Brll a) Please draw the…

A: this cis form of compound is e ,a position cause 1,3 di axial repulsion. Which decrease the…

Q: For the following conformer, draw a Newman projection looking down the 1,2 (red) bond.

A: Given is organic compound.

Q: F) Circle the letter corresponding to the relationship of each pair of structures: Identical (I),…

A: Enatiomers have non superimposable mirror image relationship. When One isomer have absolute…

Q: 3. Draw both chair conformations of the six membered rings below and circle the lowest energy…

A: While converting a six-membered cylohexane ring from any 1D representation to its chair…

Q: Draw the most stable chair conformation of the following compound: ||| ... O OH

A: The objective is to draw the most stable conformer of the tri-substituted cyclohexane. The…

Q: Predict the most stable conformation for each of the following molecules Briefly explain why your…

A: While finding out the most stable chair conformation of substituted cyclohexane, first identify all…

Q: Identify the types of strain present in this conformer. "Me" stands for "methyl". Me H H Me Me H no…

A: Torsional strain - torsional strain is applied when two groups on both the carbon are eclipsed to…

Q: What is the total strain energy of 2-methylpropane in an eclipsed conformation? (Use Newman…

A: Eclipsed Newman projection formula contain one H↔H eclipsed interaction and two H↔CH3 eclipsed…

Q: Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed…

Q: [References] Specify the types of strain that destabilize the conformer shown below. Hint: All bonds…

A: Given is organic compound.Given structure is of butane.All bonds are in Staggered conformation.

Q: Naming the compound when in trans and cis conformation please explain

A: In this question we have to tell the name of the compound.

Q: Draw the Newman projections for one staggered and one eclipsed conformation of the molecule below,…

A: The groups present on the wedge bond is written on the right and the groups present on the dash bond…

Q: Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed…

A: During Newman Projection drawing, we see along the carbon-carbon bond. To visualize the three…

Question

Draw the Newman projections for the most and least stable conformations and indicate what strain(s) the least stable conformation has. Look in the direction of arrow.

This is the structural formula for (R)-3-Fluoro-3-methyl-2-butanol, an organic compound.

### Explanation:

- **Carbon Backbone**: The structure includes a four-carbon chain. The main chain appears in a zigzag line format, which is typical for organic line structures.

- **Functional Groups**:
- The hydroxyl group (OH) is attached to the second carbon in the chain.
- There is a fluorine atom (F) attached to the third carbon in the chain.

- **Stereochemistry**:
- The structure includes wedge-and-dash notation to indicate stereochemistry.
- The solid wedge (pointing towards the viewer) indicates that the group (a CH3 group) is coming out of the plane of the page.
- The dashed line (pointing away from the viewer) indicates that the fluorine atom is going into the plane of the page.
- This configuration suggests that it is the R-enantiomer of 3-fluoro-3-methyl-2-butanol.

- **Branches**:
- There is a methyl group (CH3) attached to the third carbon, supporting the complexity of the structure.

This compound can have various applications and relevance in organic chemistry, studying enantiomers, and understanding stereochemistry.

Expert Solution

Step 1

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Similar questions

Draw both chair Conformers of chlorocylohexane. How much higher in energy is the less stable Conformer?
Draw Newman projects of all the staggered conformations for the molecule below looking along the bolded bond in the direction indicated by the arrow. The carbon closest to the arrow should be the front carbon of your Newman projection. (It is a practice problem from the book but I am confused about how to approach it.)
Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond.
Draw both a chair confirmation of the substitutes cyclohexane drawn below. Be certain to actually do a ring flip. Also be certain to very clearly distinguish axial from equatorial positions. Then circle the more stable conformation.
Solve both please neat and clean...
Same 9) a) Draw the most stable chair conformation of cis-1,2-dimethylcyclohexane. b) Calculate the energy of this structure.
Problem: Perform a conformational analysis 2-iodo-2-methylbutane, looking down the C2—C3 bond. Pay attention to the relative energies of the various conformations, but do not concern yourself with the actual energy values. Pleae draw newman projections.