Answer:
Explanation:
In this case we want to know the structures of A (C6H12), B (C6H13Br) and C (C6H14).
A and C reacts with two differents reagents and conditions, however both of them gives the same product.
Let's analyze each reaction.
First, C6H12 has the general formula of an alkene or cycloalkane. However, when we look at the reagents, which are HBr in ROOR, and the final product, we can see that this is an adition reaction where the H and Br were added to a molecule, therefore we can conclude that the initial reactant is an alkene. Now, what happens next? A is reacting with HBr. In general terms when we have an adition of a molecule to a reactant like HBr (Adding electrophyle and nucleophyle) this kind of reactions follows the markonikov's rule that states that the hydrogen will go to the carbon with more hydrogens, and the nucleophyle will go to the carbon with less hydrogen (Atom that can be stabilized with charge). But in this case, we have something else and is the use of the ROOR, this is a peroxide so, instead of follow the markonikov rule, it will do the opposite, the hydrogen to the more substituted carbon and the bromine to the carbon with more hydrogens. This is called the antimarkonikov rule. Picture attached show the possible structure for A. The alkene would have to be the 1-hexene.
Now in the second case we have C, reacting with bromine in light to give also B. C has the formula C6H14 which is the formula for an alkane and once again we are having an adition reaction. In this case, conditions are given to do an adition reaction in an alkane. bromine in presence of light promoves the adition of the bromine to the molecule of alkane. In this case it can go to the carbon with more hydrogen or less hydrogens, but it will prefer the carbon with more hydrogens. In this case would be the terminal hydrogens of the molecules. In this case, it will form product B again. the alkane here would be the hexane. See picture for structures.
Answer:
yes what do you need with
Answer:
Uses nuclear reactions to produce energy
Implodes a fuel pellet
Explanation:
Laser fusion is a method of initiating nuclear fusion reactions through heating, and compressing fuel pellets containing deuterium and tritium using high energy density laser beams. Lase fusion is also known as inertial confinement fusion and the energy produced by the process is known as Laser Inertial Fusion Energy, LIFE.
During the process of laser fusion, small pellets of deuterium-tritium (DT) isotopes mixture are fed into a blast chamber where they are compressed to high densities using a number of amplified laser beams in the chamber.
The high energy density of the beams as well as the heat produced due to compression, induces the thermonuclear explosion ignition resulting in the production of high energetic products such as charged particles, x-rays and neutrons. The energy produced is absorbed and stored as heat in a blanket that is then used in a steam thermal cycle to generate electrical power.
There are two methods of compression of the DT pellet: direct and indirect-drive laser fusions.
However, there are a number of limitations to energy production by this process. One limitation is that the process is extremely inefficient in energy energy production. Also, the heat produced by the flashtubes results innthe deformation of the laser glass.
Tin(II) fluoride or stannous fluoride
the reagents necessary to convert alcohol to ketone
which involves oxidation of alcohols.
<h3>
What is oxidation of alcohols?</h3>
- Alcohol oxidation is a significant organic chemistry process. Secondary alcohols can be oxidized to produce ketones, while primary alcohols can be oxidized to produce aldehydes and carboxylic acids.
- In contrast, tertiary alcohols cannot be oxidized without the C-C bonds in the molecule being broken.
- In order to cause primary alcohols to oxidize into aldehydes
(dichromate)
/pyridine (Collins reagent)- Chromium pyridinium compound (PCC)
- Dichromate of pyridinium (PDC, Cornforth reagent)
- Periodinane by Dess-Martin
- Oxalyl chloride with dimethylsulfoxide (DMSO) for Swern
- oxidation of secondary alcohols to ketones
- (dichromate)
- /pyridine (Collins reagent)
- Chromium pyridinium compound (PCC)
- Dichromate of pyridinium (PDC, Cornforth reagent)
- Periodinane by Dess-Martin
- Oxalyl chloride and dimethyl sulfoxide (DMSO) (Swern oxidation)
/acetone (Jones oxidation)- Acetone with aluminum isopropoxide (Oppenauer oxidation)
To learn more about oxidation of alcohols with the given link
brainly.com/question/7207863
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<u>Question:</u>
Identify the reagents necessary to achieve each of the following transformations
