<span>When cyclohexanol is dehydrated using various means it creates a new hydrocarbon. This new hydrocarbon is called cyclohexene. Cyclohexene is a liquid which has no color, yet has a very strong smell to it. It is used in common industrial processes, but is also considered somewhat unstable due to it's tendency to form peroxides when exposed to light.</span>
140 s. It would take 140 s to swim 0.150 mi
.
<em>Step 1</em>. Convert the <em>time to seconds</em>
Time = 14 min × (60 s/1 min) + 34.56 s = 840 s + 34.56 s = 874.56 s
<em>Step 2</em>. Convert <em>miles to metres
</em>
Distance = 0.150 mi × (1609.3 m/1 mi) = 241.4 m
<em>Step 3.</em> Calculate the <em>time to swim 241.4 m</em>
Time = 241.4 m × (874.56 s/1500 m) = 140 s
(<em>As of 2012, the men’s freestyle record for 1500 m was 14:31.02</em>.)
I think it is C. coefficients but I don't know what subscripts are
Prontosil is a compound produced by the coupled reaction of an aryldiazonium ion and an aromatic compound.
<h3>
What are diazonium compounds?</h3>
These are organic compounds in which there are ionic interactions between the azo group (-N₂⁺) and an anion X⁻.
The general structure is RN₂⁺X⁻.
- R is the lateral chain that might be an aromatic ring, among other options.
The azo group characterizes as being unstable and reactive. This property is because one of the N atoms has a positive charge.
-N⁺≡ N
<h3>What is the coupling reaction of aryldiazonium compounds?</h3>
Aryldiazonium salt reactions can occur in two ways,
- Substitution reactions
- Coupling reactions
Coupling reactions are the aromatic electrophilic substitution, where the aryldiazonium ion acts as an electrophile for an activated aromatic compound to attack it.
The coupling reaction occurs at the azo group level.
In the exposed example,
- the benzene ring with sulfur bonded to oxygen atoms is the coupling component
- the benzene ring with NH₂ and the azo group is the diazonium ion
In the attached files you will find the drawings.
You can learn more about diazonium compounds at
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