Answer:
<u><em>See attachment for explanations.</em></u>
Explanation:
Oxygen and carbon dioxide
Answer:
Explanation:
Hello,
In this case, due to the volume displacement caused the by the object's submersion, it's volume is:
In such a way, considering the mathematical definition of density, it turns out:
Rounding to the nearest tenth we finally obtain:
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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:
Uranium-238 undergoes alpha decay to form Thorium-234 as daughter product.
Explanation:
Alpha decay is indicative of loss of the equivalents of a helium particle emission. The reaction equation for this reaction is shown below:
→
I hope this explanation is clear and explanatory.