Answer:
The final volume in mL is 7.14 mL or 7.1 mL.
Explanation:
1.Use Boyle's Law(
). Re-arrange to solve for
<em> for the final volume.</em>
<em />
<em>2. Plug in values. </em>
Explanation:
When a carboxylic acid is treated with an alcohol and an acid catalyst, an ester is formed (along with water). This reaction is called the Fischer esterification.
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When finding the chemical formula of a compound, we will need to find the charges of each element/bond.
Looking at our period table, sodium has a +1 charge, written as Na 1+, and sulfate has a charge of -2, and it is written as SO4 2-.
Now, we need to make the charges equivalent. To do this, we need to "criss-cross" the charges. This means that sodium will need to additional atoms to make the charges equal, and sulfate will need one.
Therefore, the chemical formula for sodium sulfate is: Na2SO4.
A neutralization titration is a chemical response this is used to decide the composition of an answer and what kind of acid or base is in it. This is a way of volumetric analysis and the formula is (
).
Utilize the titration method of
in view that we're given the concentrations of every compound and the quantity of
. Let: M1 = 0.138M, V1 = x, M2 = 0.205M, V2 = 26.0 ML.
- M1 = initial mass
- V1= initial volume
- M2 = final mass
- V2= final volume

- (0.138)(V1) = (0.205)x(26.0)
- V2=(0.205)x(26.0)\ 0.138
- V2 = 47.10 M/L
- The final value of Volume needed for neutralization of nitric acid solution is V2 = 47.10 M/L
Read more about the neutralization:
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Answer:
IV
Explanation:
The complete question is shown in the image attached.
Let us call to mind the fact that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.
Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.
Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic substitution reaction by SN1 mechanism.