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:
gametes are sperm and an egg individually. when the gametes come together and fertilize, they form a zygote.
Answer:The environmental problems directly related to energy production and Electricity is a secondary energy source that is generated producedfrom primary energy sources:
hope that helps im new so have a good day (:
Explanation:
Answer:
Kb = 6.22x10⁻⁷
Explanation:
Triethanolamine, C₆H₁₅O₃N, is in equilibrium with water:
C₆H₁₅O₃N(aq) + H₂O(l) ⇄ C₆H₁₅O₃NH⁺(aq) + OH⁻(aq)
Kb is defined from concentrations in equilibrium, thus:
Kb = [C₆H₁₅O₃NH⁺] [OH⁻] / [C₆H₁₅O₃N]
The equilibrium concentration of these compounds could be written as:
[C₆H₁₅O₃N] = 0.486M - X
[C₆H₁₅O₃NH⁺] = X
[OH⁻] = X
pH is -log [H⁺], thus, [H⁺] = 10^-pH = 1.820x10⁻¹¹M
Also, Kw = [OH⁻] ₓ [H⁺];
1x10⁻¹⁴ = [OH⁻] ₓ [H⁺]
1x10⁻¹⁴ = [OH⁻] ₓ [1.820x10⁻¹¹M]
5.495x10⁻⁴M = [OH⁻], that means <em>X = 5.495x10⁻⁴M</em>
Replacing in Kb formula:
Kb = [5.495x10⁻⁴M] [5.495x10⁻⁴M] / [0.486M-5.495x10⁻⁴M]
<em>Kb = 6.22x10⁻⁷</em>
<em></em>
