Rank these conformational isomers in order of decreasing potential energy?

Highest on the left and lowest on the right. To rank items as equivalent, overlap them.

Here is a link to the picture of the problem:

ht+tp+:/+/bit+.ly/+8ZHeDA Remove the '+' sign

I'm sorry, but I cannot access external links or view pictures. However, I can still help you understand the concept of potential energy in conformational isomers!

In general, potential energy in conformational isomers is influenced by the stability of the molecule. The more stable a conformation, the lower its potential energy. Without seeing the pictures, I can provide you with some general guidelines:

1. Look for any interactions or clashes between atoms or groups in each conformation. If there are significant clashes, it usually indicates a higher potential energy.

2. Consider the type of strain present in each conformation. For example, if there is torsional strain or steric hindrance, it generally results in higher potential energy.

3. If there are any stabilizing factors, such as intramolecular hydrogen bonds or favorable interactions between atoms or groups, it can lead to a lower potential energy.

Remember, these are just general guidelines, and without specific information about the conformational isomers, it's difficult to give a definitive ranking.

I'm sorry, but as an AI text-based bot, I am unable to access or view external links or pictures. However, I can help explain the concept and provide general guidance on ranking conformational isomers based on potential energy.

When ranking conformational isomers based on potential energy, it is important to consider the stability of each isomer. Generally, more stable isomers have lower potential energy.

Here are some general guidelines:

1. Fully eclipsed: This is the least stable conformational isomer, commonly found in rotation around single bonds where there is maximum steric hindrance. It has the highest potential energy.

2. Eclipsed: This is another unstable conformational isomer where there is partial overlap (eclipsing) of the atoms or groups attached to the neighboring atoms. It has relatively higher potential energy compared to other isomers.

3. Gauche: This conformational isomer is more stable as compared to fully eclipsed and eclipsed isomers, but less stable than the other isomers mentioned below.

4. Anti: This is a relatively stable conformational isomer where the groups attached to neighboring atoms are opposite to each other. It is more stable than the previous three isomers.

5. Staggered: This is the most stable conformational isomer where there is maximum separation between the atoms or groups attached to neighboring atoms. It has the lowest potential energy among the mentioned isomers.

Remember that these guidelines are general, and the stability of conformational isomers can vary depending on the specific molecule and the interactions of its substituents.

If you provide more specific information about the molecule or isomers in question, I can try to provide a more accurate ranking based on the information given.

To rank these conformational isomers in order of decreasing potential energy, we need to analyze the stability of each isomer. However, I'm sorry, but as an AI text-based model, I am unable to access external links or view images. Therefore, I won't be able to see the picture you mentioned.

However, I can still guide you on how to approach this problem. To determine the relative potential energy of conformational isomers, you need to consider the following factors:

1. Steric Strain: Evaluate the steric interactions or clashes between substituents on adjacent atoms. Bulkier substituents will generally lead to increased steric strain and higher potential energy.

2. Torsional Strain: Assess the energy associated with eclipsing or gauche interactions between substituents on adjacent atoms. Eclipsing interactions increase torsional strain, which contributes to higher potential energy.

3. Dipole-Dipole Interactions: Consider polar bonds and the potential energy associated with interactions between partial charges. If there are regions of high electron density close together, there may be increased electrostatic repulsion, leading to higher potential energy.

Using the provided picture, you can visually analyze these factors for each isomer. Identify any steric and torsional strains by noting the proximity and arrangement of substituents. Additionally, consider whether there are any polar bonds or large differences in electronegativity that could contribute to dipole-dipole interactions.

Once you have evaluated these factors for each conformational isomer, compare them to determine their relative potential energy. The isomers with the highest steric and torsional strains and significant dipole-dipole interactions will generally have the highest potential energy, while those with fewer or no such interactions will have lower potential energy.

Without directly viewing the picture, I'm unable to provide you with the specific order of the conformational isomers. If you have any further questions or need additional assistance, feel free to ask.

4,2,3-5,1

Three and five equivalent so overlap.