Pure- table salt
Impure- vegetable oil
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
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<u>Answer:</u> The number of moles of weak acid is
moles.
<u>Explanation:</u>
To calculate the moles of KOH, we use the equation:

We are given:
Volume of solution = 43.81 mL = 0.04381 L (Conversion factor: 1L = 1000 mL)
Molarity of the solution = 0.0969 moles/ L
Putting values in above equation, we get:

The chemical reaction of weak monoprotic acid and KOH follows the equation:

By Stoichiometry of the reaction:
1 mole of KOH reacts with 1 mole of weak monoprotic acid.
So,
of KOH will react with =
of weak monoprotic acid.
Hence, the number of moles of weak acid is
moles.
Answer:
its shorter than a regular one
Explanation:
the only reason is simply because it is shorter