Linked Questions

3
votes
1answer
2k views

Are resonating structures real or not? [duplicate]

We say that hybrid structure is real. It has distinct properties as compared to its Resonating Structure. Is it because that all the experiments we carry out are on a sample, lots of molecules are ...
3
votes
1answer
672 views

Resonance in ozone and benzene [duplicate]

In inorganic chemistry, I learnt that stability of some atoms like ozone cannot be explained by one structure alone and hence the hybrid of possible structures is taken and assumed to be the structure ...
10
votes
4answers
1k views

Does benzene structure stand for a single resonance form or the whole molecule?

It is known that benzene has two main resonance forms Often we still draw benzene molecule as one of them My question is, actually when we draw the lower figure, do we refer to the whole benzene ...
22
votes
3answers
660 views

What is the isomer distribution in monosubstituted fluorobullvalene?

Bullvalene (tricyclo[3.3.2.02,8]deca-3,6,9-triene) is a fluxional molecule able to interconvert any two carbon atoms through a series of degenerate Cope rearrangements (for more information, see the ...
13
votes
6answers
46k views

How to determine the least stable resonance structures out of a given set?

So I was "happily" doing organic chemistry homework when I came across this question: For 1-methoxy-1,3-butadiene, which of the following resonating structure is the least stable? $$\begin{...
16
votes
2answers
581 views

What are the important implications to the field of chemistry, if any, of the recently confirmed hexavalent carbon species?

I’m struggling to understanding the true nature and implications of recent confirmations of the existence of stable species containing carbon atoms bound six (in another case 5) other carbon atoms. Is ...
8
votes
3answers
3k views

Rearrangement of double bonds

Consider: I found these rearrangements, but I could not understand what the mechanism is behind this. When I searched on the Internet I found the Wikipedia page Di-pi-methane rearrangement.
6
votes
1answer
14k views

Structures for NO+ (Nitrosonium)

There are two possible structures for Nitrosonium : In the first structure, there is a +1 Formal charge on Oxygen, whereas, In the second structure, there is a +1 Formal charge on Nitrogen. Q. ...
7
votes
2answers
3k views

What is the “resonance hybrid” of benzene?

In my book, to explain the structure of benzene, it referred to the idea of resonance: The idea of resonance is that the actual molecule is a definite structure that is a hybrid of two or more ...
5
votes
2answers
4k views

What is the most “important” resonance structure of SCN⁻?

Numerous online references say that $\ce{SCN-}$ has two resonance structures: I am wondering why this structure is not also possible? I expect structure 3 to be rare because of the high formal ...
8
votes
2answers
647 views

Trying to understand the statement: 'Resonance is not a flickering between the contributing states. '

So, the famous resonance definition: it is the weighted average of different Lewis structures.... Well, this is purely wrong. Resonance is nothing but quantum 'superposition of the wavefunctions ...
6
votes
1answer
6k views

What is the order of stability of the resonance structures of furan?

I want to know which are the most stable furan resonance structures. I know that structure number 1 is the most stable, but which one comes after?
7
votes
3answers
3k views

Why does HNO2 not have resonance?

A question on the 1996 AP Chemistry Free Response asks: The $\ce{N-O}$ bonds in the $\ce{NO2-}$ ion are equal in length, whereas they are unequal in $\ce{HNO2}$. Explain. Since the nitrogen ...
2
votes
2answers
772 views

Stability and resonance structures

In school they ask us to count the number of resonance structures in different organic compounds to determine it's stability. The one with more resonance structures is more stable. Is this notion ...
3
votes
1answer
3k views

How to explain (non-/anti-) aromaticity in fulvene with the help of resonance structures?

Can someone please explain why the resonance structures of fulvene 1 is non-aromatic and 2 is anti-aromatic? Why is fulvene non-aromatic, even though it has $4\pi$-electrons and no $\mathrm{sp^3}$ ...

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