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Questions tagged [halides]

Chemical compounds that contain halogens (group 17 in the Periodic Table) as part of their chemical structure. This tag should only be applied where the halide group is one of the main focuses of the question.

1 vote
0 answers
84 views

Why is the melting point of meta-diiodobenzene higher than that of ortho-diiodobenzene?

I'm currently trying to reason for as why the melting point of meta-diiodobenzene higher than that of ortho-diiodobenzene and I'm unsure of what to say. I understand the para isomer has the highest ...
bigmannus's user avatar
-6 votes
1 answer
54 views

Formation of carbocation on reaction with strong acid in presence of halogen [closed]

Shouldn't the carbocation be formed away from the -I effect of the Cl atom for more stability. Backbonding is achieved in a later step after hydride shift.
Meet Shah's user avatar
1 vote
0 answers
43 views

Will benzyl halides undergo SN1 or SN2 mechanism in a polar aprotic solvent?

If benzyl bromide reacts with KF in the presence of a polar aprotic solvent like DMF, will it undergo SN1 mechanism or SN2 mechanism ? I understand that polar aprotic solvents favour SN2 mechanism but ...
standardsolution's user avatar
2 votes
2 answers
241 views

Does ferrocenium chloride ([Fe(C5H5)2]Cl) exist as a stable compound?

I am interested in using ferrocenium chloride ($\ce{[Fe(C5H5)2]Cl}$) for a synthesis application, but I couldn't find any sources referring to its existence, even though some websites and a figure in ...
psansoldo's user avatar
6 votes
1 answer
113 views

Whatever happened to the use of perfluoroalkanes as breathable liquids or blood substitutes?

Some liquid perfluoroalkanes have very high solubilities and carrying capacities for gases like oxygen and carbon dioxide. In the 1980s and 1990s there were experiments showing that animals could &...
matt_black's user avatar
0 votes
2 answers
208 views

What is meant by 'as Cl2'

I feel like I'm over thinking this one, but think I need a confirmation (and quantified example) to put my confusion to bed. I'm more a mechanical than chemical background but trying my best. I really ...
Kuhrta's user avatar
  • 65
-3 votes
1 answer
123 views

Constituents of LaI2 [closed]

An ionic solid $\ce{LaI2}$ shows electrical conduction due to presence of which anions and cations?
WATCHER's user avatar
1 vote
1 answer
125 views

Why doesn’t the reaction between 3-mercaptopropionic acid and methyl iodide yield a methyl ester? [closed]

Problem Answer Question I don’t understand why 3‐methylthiopropionic acid (X) is the correct answer. Wouldn’t sulfur and carbon have similar electronegativities? As the consequence, isn’t it more ...
nmrislife's user avatar
0 votes
0 answers
32 views

Solubility of fluoroalkanes [duplicate]

I know haloalkanes generally aren't soluble in water due to their inability to form hydrogen bonds in water, despite being moderately polar. I was wondering why this is the case with fluoroalkanes too ...
Baishnavi Prasad's user avatar
0 votes
0 answers
697 views

Weight Ratio vs Molar Ratio - Chloramines

I'm working with a delicate experiment whilst trying to test corrosion of stainless-steels in a chloramine environment. I've run into various literature that discusses the formation of different types ...
Kuhrta's user avatar
  • 65
2 votes
0 answers
146 views

Chloramines & Nitrogen Trichloride vs Stainless Steel [closed]

We've recently experienced excessive corrosion on stainless steel within indoor pool environments. We believe this is due to chloramine (gasses) in the atmosphere. To test this, I plan to create a ...
Kuhrta's user avatar
  • 65
1 vote
1 answer
462 views

Substitution or elimination when a chloroalkene reacts with NaOH in ethanol?

NaOH + EtOH will eliminate the Cl atom forming a double bond. At least, that's what I think. 3 could also be a viable answer since the OH can also attack the said double bond (this is probably not ...
Aranya's user avatar
  • 13
0 votes
0 answers
36 views

Why 2-methyl-1-propene's halohydrin formation does not involve steric effect?

This concerns Marc Loudon's Organic Chemistry 6th Edition's 5.2 page 187. Consider 2-methyl-1-propene and its halohydrin formation mechanism. Usually, there will be formation of bromonium, where I ...
user45765's user avatar
  • 101
6 votes
4 answers
2k views

How to distinguish silver chloride, bromide and iodide?

When we test for chloride, bromide and iodide ions we use the obvious silver nitrate and dilute nitric acid test. However distinguishing between the precipitates is often quite tricky. How can we tell ...
Goffried Leibniz's user avatar
3 votes
1 answer
217 views

Free-radical addition of bromine to alkene

If light and radical initiators are present, radical addition of $\ce{HBr}$ to alkenes takes place and outcompetes electrophilic addition of $\ce{HBr}$ to alkenes. Why isn't a similar thing same ...
Silenus's user avatar
  • 41

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