Answer:
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<span>A. Commercial cooking
</span>
Answer:
element
Explanation:
an element is something made up of only one type of atom
Explanation:
The given data is as follows.
Weight of solute = 75.8 g, Molecular weight of solute (toulene) = 92.13 g/mol, volume = 200 ml
- Therefore, molarity of toulene is calculated as follows.
Molarity = 
= 
= 4.11 M
Hence, molarity of toulene is 4.11 M.
- As molality is the number of moles of solute present in kg of solvent.
So, we will calculate the molality of toulene as follows.
Molality = 
= 
= 8.6 m
Hence, molality of given toulene solution is 8.6 m.
- Now, calculate the number of moles of toulene as follows.
No. of moles = 
= 
= 0.8227 mol
Now, no. of moles of benzene will be as follows.
No. of moles = 
= 
= 1.2239 mol
Hence, the mole fraction of toulene is as follows.
Mole fraction = 
= 
= 0.402
Hence, mole fraction of toulene is 0.402.
- As density of given solution is 0.857
so, we will calculate the mass of solution as follows.
Density = 
0.857
=
(As 1
= 1 g)
mass = 171.4 g
Therefore, calculate the mass percent of toulene as follows.
Mass % = 
= 
= 44.22%
Therefore, mass percent of toulene is 44.22%.
The correct option is (b)
NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').
Learn more about NANH2 here :-
brainly.com/question/12601787
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