Knowee
Questions
Features
Study Tools

There are Choose your answer here resonance structures that can be drawn for the cyclopentadienyl cation.

Question

There are Choose your answer here resonance structures that can be drawn for the cyclopentadienyl cation.

🧐 Not the exact question you are looking for?Go ask a question

Solution

The cyclopentadienyl cation, C5H5+, is a cyclic compound with 5 carbon atoms and 5 hydrogen atoms. It has a positive charge due to the loss of one electron.

Step 1: Draw the basic structure of the cyclopentadienyl cation. It is a pentagon with a positive charge.

Step 2: Identify the pi electrons. In the cyclopentadienyl cation, there are 4 pi electrons.

Step 3: Draw the resonance structures. Resonance structures are alternate ways of drawing a molecule without changing the location of the atoms. In the case of the cyclopentadienyl cation, you can draw two resonance structures.

In the first structure, the double bonds can be placed between the first and second carbon atoms, and between the third and fourth carbon atoms.

In the second structure, the double bonds can be placed between the second and third carbon atoms, and between the fourth and fifth carbon atoms.

So, there are 2 resonance structures that can be drawn for the cyclopentadienyl cation.

This problem has been solved

Similar Questions

A total of how many resonance structures can be drawn for the cyclopentadienyl anion?Select answer from the options below56342

Write the resonance structures of hydrogenchloride. Which of these structures is themost important one ?

A resonance structure is best defined as occurring when . The bond length that occurs in a bond that exhibits resonance will .

Which is not aromatic 1) teopyliumcation 2) chrysene 3) cyclopentadienyl 4) cyclopropenyl

The structure of 4-Methylpent-2-en-1-ol is: (a) CH3CH2CH=CHCH2OH(b)(CH3)2C=CHCH2CH2OH (c)(CH3)2CHCH=CHCH2OH(d)CH3CH(OH)CH-CH=C(CH3)2.

1/1

Upgrade your grade with Knowee

Get personalized homework help. Review tough concepts in more detail, or go deeper into your topic by exploring other relevant questions.