Answer:
C
Explanation:
Because on the moon you are basically weightless and your mass would stay the same
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:
NH₃ (Option A)
Explanation:
Arrhenius theory explained that the acids are the ones that have H⁺, either H in its formula. Following this, the bases are the ones that have OH⁻ , either OH and its formula.
It can be used only with compounds with H, or OH.
So the ammonia is not a base, as Arrhenius theory.
It is known that ammonia behaves as a weak base, but it does not have hydroxide ions that can yield to water
Answer:
Protons:
- positive
- aka cation
- in the nucleus along with the neutrons
Electrons:
- negative
- aka anion
- situated in the orbital shells/configuration levels (there are many names)
FLOOR. Most of the molecules that dont sick to something fall on the floor so most would be on the FLOOR.
