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:
I will say D. The molecules become arranged into regular cubic arrangement. but i'm not 100% sure
Explanation:
A eukaryotic cell goes through nuclear division creating two identical daughter cells.
Answer:
layer B is liquid because of the inner members and layer A is solid because of the outer members
Answer:
The answer is
<h2>126.58 mL</h2>
Explanation:
The volume of a substance when given the density and mass can be found by using the formula
<h3>
</h3>
From the question
mass of alcohol = 100 g
density = 0.79 g/mL
The volume is
We have the final answer as
<h3>126.58 mL</h3>
Hope this helps you
