1answer.
Ask question
Login Signup
Ask question
All categories
  • English
  • Mathematics
  • Social Studies
  • Business
  • History
  • Health
  • Geography
  • Biology
  • Physics
  • Chemistry
  • Computers and Technology
  • Arts
  • World Languages
  • Spanish
  • French
  • German
  • Advanced Placement (AP)
  • SAT
  • Medicine
  • Law
  • Engineering
Sauron [17]
1 year ago
6

Select all the statements that correctly describe the chair conformation of cyclohexane. Multiple select question. The bond angl

es are near 109.50. Each carbon atom has one axial and one equatorial hydrogen atom. All hydrogen atoms on adjacent carbon atoms are staggered. The chair conformation is less stable than the boat conformation.
Chemistry
1 answer:
Yuki888 [10]1 year ago
8 0

All the statements except Option D is true for the chair confirmation of cyclo hexane.

<h3>Describe the Chair confirmation of Cyclohexane  ?</h3>

The flexibility of Cyclo hexane allows for formation of a confirmation ,

This confirmation has lowest energy among the confirmations that can be made for Cyclohexane.

The bond angles are near 109.50 degree,

Each carbon atom has one axial and one equatorial hydrogen atom and All hydrogen atoms on adjacent carbon atoms are staggered.

Therefore Option A , B , C are all true statements about the Chair Confirmation of Cyclohexane.

To know more about Chair Confirmation

brainly.com/question/14852324

#SPJ1

You might be interested in
Lord kelvin described the concept of absolute zero temperature and the laws relating the change in thermal energy during chemica
kondaur [170]
Lord Kelvin, were he alive today, would be considered a Thermochemist. Thermochemistry is interested in the role of heat in chemical reactions. This includes the role of heat both as a biproduct of chemical reactions and a facilitator.

Kelvin's description of absolute zero is an important concept in thermochemistry. At absolute zero, there is no movement of molecules, and no energy available facilitate chemical reactions. 
6 0
2 years ago
Using the Erlenmeyer flask and its contents from part A, continue with
Anestetic [448]
It’s b for sure that’s the answer
5 0
2 years ago
Read 2 more answers
Rank the solutions in order of decreasing [H3O ]. Rank solutions from largest to smallest hydronium ion concentration. To rank i
Usimov [2.4K]

Answer:

0.10M HCN  <  0.10 M HClO  <  0.10 M HNO₂  < 0.10 M HNO₃

Explanation:

We are comparing acids with the same concentration. So what we have to do first is to determine if we have any strong acid and for the rest ( weak acids ) compare them by their Ka´s ( look for them in reference tables ) since we know the larger the Ka, the more Hydronium concentration will be in these solutions at the same concentration.

HNO₃ is a strong acid and will have the largest hydronium concentration.

HCN  Ka = 6.2 x 10⁻¹⁰

HNO₂ Ka = 4.0 x 10⁻⁴

HClO  Ka = 3.0 x 10⁻⁸

The ranking from smallest to largest hydronium concentration will then be:

0.10M HCN  <  0.10 M HClO  <  0.10 M HNO₂  < 0.10 M HNO₃

5 0
3 years ago
When methyloxirane is treated with HBr, the bromide ion attacks the less substituted position. However, when phenyloxirane is tr
konstantin123 [22]

Answer:

See explanation and picture below

Explanation:

First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.

In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.

In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.

4 0
3 years ago
Which number represents an acidic pH, 4 or 9?
Leno4ka [110]

Answer:

pH 4 represents an acidic

5 0
3 years ago
Other questions:
  • What is the main point of the reading?
    10·2 answers
  • For the reaction
    15·2 answers
  • In nature, where do fusion reactions take place?
    13·1 answer
  • A mineral contains only a metal, M, and sulfur. If analysis indicates that a 4.3 g sample of the mineral contains 1.56 g of M, w
    8·1 answer
  • A commercial oven with a book value of $67,000 has an estimated remaining 5 year life. A proposal is offered to sell the oven fo
    13·1 answer
  • According to Bowen's reaction series, crystal settling should result in the magma being separated in lower layers rich in the ea
    6·1 answer
  • You are trying to remove small particles from water. What would be the BEST thing you could do to remove the small particles? *
    9·1 answer
  • Which organisms in soil helps relieve element so they can be recycled
    13·2 answers
  • Riley let his friend borrow $12,750. He wants to be paid back in 57 months and is going to charge his friend a 5.5% interest rat
    15·1 answer
  • Why are metals so ductile?
    8·1 answer
Add answer
Login
Not registered? Fast signup
Signup
Login Signup
Ask question!