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.
Explanation:
False, gray whales average 75 miles per day at a speed of 5 mph and is the longest annual migration of any mammal.
Answer:
the mass of the glass is 2
<h3>
Answer:</h3>
Single displacement reaction
<h3>
Explanation:</h3>
- Single replacement reaction is a type of reaction in which a reactive element displaces a less reactive element from its compound.
- The reaction given above; Al + H₂SO₄ → Al₂(SO₄)₃ + H₂ is a single replacement reaction.
- This is because Aluminium takes the place of hydrogen atoms in sulfuric acid to form aluminium sulfate and hydrogen gas.
- Double replacement reaction is where cations or anions are exchanged between two compounds to form new compounds.
- For example the reaction; NaCl(aq) + AgNO₃(aq) → NaNO₃(aq) + AgCl(aq) is a double displacement reaction.
Answer:
Kinetic Energy
Explanation:
Kinetic energy is the energy inside moving objects of things.
