Make an observation.
Conduct research.
Form hypothesis.
Test hypothesis.
Record data.
Draw conclusion.
Replicate.
One thing that is designed to change in the set up of the experiment. ( The things that I can change) Independent Variable.
Answer:
The rocket is now too heavy to reach its destination.
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.
They're only found in the nucleus and play an important role in keeping the atom stable because they carry a negative charge to counteract the proton's positive charge.
