Why Do Resonance Structures for ClO- and ClO4- Differ in Formal Charges?

  • Thread starter Thread starter MathewsMD
  • Start date Start date
  • Tags Tags
    Structures
AI Thread Summary
Resonance structures for ClO- show two configurations, one with oxygen carrying a -1 charge and another with chlorine at -1, despite oxygen's higher electronegativity. The average bond order for ClO- is calculated to be 1.5, while ClO4- has an average bond order of 7/4, explaining the absence of a fifth resonance structure with chlorine holding a negative charge. The discussion emphasizes that resonance structures are theoretical and rely on calculations rather than observable forms. It highlights the ionic nature of bonding in these compounds, indicating that covalent double bonds between Cl and O do not exist. Understanding average bond order can involve methods beyond Lewis structures, reflecting the complexity of bonding in higher main group compounds.
MathewsMD
Messages
430
Reaction score
7
Hi,

When drawing the resonance structures for ClO-, two exist. One where the O has a formal charge of -1 and there is then a single bond. The other structure is Cl with -1 for formal charge. Why is this second structure an equal resonance structure (why does the Cl have a negative formal charge) when O has the higher electronegativity?

Also, my next question stem from the previous one. In ClO4-, you have 4 resonance structures where the negative formal charge alternates between the 4 oxygen atoms, and the average bond order is 7/4. Why does a fifth resonance structure not exist where the chlorine has the negative formal charge, and makes a double bond with EACH oxygen atom?

It seems like Cl can have a negative formal charge in ClO- and not ClO4-, and I would like an explanation for that, if possible.

Thanks!
 
Chemistry news on Phys.org
This are good questions. As resonance structures aren't observable experimentally, you have to rely on calculations. If you look at these, there is in fact no double bond between Cl and O and O is either neutral or carries a negative formal charge.
 
DrDu said:
This are good questions. As resonance structures aren't observable experimentally, you have to rely on calculations. If you look at these, there is in fact no double bond between Cl and O and O is either neutral or carries a negative formal charge.

Ok. I understand the basics of resonance structures. I realize Lewis structures are used as visual aids, and are never in this form at any time, while the actual structure is only the hybrid. Just to confirm, you're saying the calculated average bond order is 1.5 for ClO- and 7/4 for ClO4-, and that is the reason the the other possible structures are not considered, right? Are there any other molecules like ClO- where the formal negative charge in the drawn Lewis structures goes to the less electronegative atom? How about for a positive formal charge on the more electronegative atom?

Also, do you mind shedding some light on how average bond order is actually calculated using a method besides Lewis structures?
 
No, I am saying that bonding has I high degree of ionicity in these compounds and that there are certainly no covalent double bonds between Cl and O in these compounds. Bonding in higher main group compounds is not that simple. A classic is the following article, which you may obtain via your library:
http://onlinelibrary.wiley.com/doi/10.1002/anie.198402721/abstract
 
I want to test a humidity sensor with one or more saturated salt solutions. The table salt that I have on hand contains one of two anticaking agents, calcium silicate or sodium aluminosilicate. Will the presence of either of these additives (or iodine for that matter) significantly affect the equilibrium humidity? I searched and all the how-to-do-it guides did not address this question. One research paper I found reported that at 1.5% w/w calcium silicate increased the deliquescent point by...
I was introduced to the Octet Rule recently and make me wonder, why does 8 valence electrons or a full p orbital always make an element inert? What is so special with a full p orbital? Like take Calcium for an example, its outer orbital is filled but its only the s orbital thats filled so its still reactive not so much as the Alkaline metals but still pretty reactive. Can someone explain it to me? Thanks!!
I'm trying to find a cheap DIY method to etch holes of various shapes through 0.3mm Aluminium sheet using 5-10% Sodium Hydroxide. The idea is to apply a resist to the Aluminium then selectively ablate it off using a diode laser cutter and then dissolve away the Aluminium using Sodium Hydroxide. By cheap I mean resists costing say £20 in small quantities. The Internet has suggested various resists to try including... Enamel paint (only survived seconds in the NaOH!) Acrylic paint (only...
Back
Top