Do More Double Bonds in Hydrocarbons Require Higher Melting Temperatures?

  • Thread starter Thread starter nemzy
  • Start date Start date
  • Tags Tags
    Heat
AI Thread Summary
The discussion centers on the relationship between the number of double bonds in hydrocarbons and their melting points. It is established that hydrocarbons with more double bonds generally require more energy to melt compared to those with fewer or no double bonds. However, one participant points out that the melting process is more influenced by the crystalline structure and intermolecular forces rather than just the number of double bonds. The conversation also touches on the polarizability of alkenes versus alkanes, suggesting that alkenes may have higher boiling points due to stronger dispersion forces. A specific problem is presented regarding the melting temperatures of three fatty acids with varying double bonds, concluding that the hydrocarbon with no double bonds will require the least energy to melt, while the one with two double bonds will require the most.
nemzy
Messages
124
Reaction score
0
A hydrocarbon that has lots of double bonds takes more energy to melt, so therefore takes more heat than a hydrocarbon with less double bonds right?

so a hydrocarbon with no double bonds will require the least amount of energy, so the last amount of heat

is my concept right?

thanks
 
Chemistry news on Phys.org
I'm sorry,but i don't see a direct connection between the number of double bonds in a carbon compound and the liquifying latent heat.The latter has to do with the crystaline structure of the solid hydrocarbon and the intermolecular bonds and not necessarily with the intramolecular bonds.

Perhaps someone else could come up with the connection u're searching for...

Daniel.
 
Well, alkenes are generally more polarizable than alkanes, so you would expect a higher boiling point based on dispersion forces.
 
nemzy said:
A hydrocarbon that has lots of double bonds takes more energy to melt, so therefore takes more heat than a hydrocarbon with less double bonds right?
Assuming that the hydrocarbon is in a liquid form then if you heat some of it it will produce smoke. If the smoke is 'smokey' then it has more alkenes in it. If the smoke is more whispy then it has more alkanes in it.

This may not have been explained well.

The Bob (2004 ©)
 
ok, well here is the exact details of the problem:

which fatty acid melts at the highest temperature (solid to liquid)

(order from lowest to highest temp required to melt)
Don't know how to draw on here, so i will just explain it to you

1) a 17 long hydrocarbon chain with a Carboxyl group attached at the end. Has no double bond

2) a 17 long hydrocarbon chain with a Carboxyl group attached at the end. Has 1 double bond

3) a 17 long hydrocarbon chain with a Carboxyl group attached at the end. Has 2 double bonds.


My guess is that 1 requires least and 3 requires most temperature
 
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