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.
Answer:
Volume
Explanation:
Volume is how much of a substance something can hold!
Hope this helped, have a nice day! :)
Answer:
<u>CH</u>
Explanation:
Molecular formula of propene : <u>C₃H₆</u>
Take the HCF of carbon and hydrogen atoms :
Then, we can write the formula as :
- 3CH
- This means there are 3 moles present
Empirical Formula :
- Molecular Formula / No. of moles
- C₃H₆ / 3
- <u>CH</u>
<u></u>
The empirical formula of propene is <u>CH</u>
Answer:
32.23 to 4 significant figures.
Explanation:
The molar mass of the element is the mass of 6.022 * 10^23 atoms (Avogadro's number).
So by proportion it is 6.022 * 10^23 * 3.88 / 7.25 * 10^22
= 32.23 to 4 significant figures.