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:
The correct answer is A Energy leaves the iron bar and enters the wood until the temperature are equal.
Explanation:
According to the law of conservation of energy or the first law thermodynamics energy neither be created nor destroyed, energy is transferred from one form to another form.
Here iron bar is placed in wood block energy is transferred from iron bar to wood until the temperatures are equal.
Answer:
a. magnesium
b. nitrogen
Explanation:
Barium and magnesium are both in 2nd group, so most similar compounds.
Nitrogen - 15 group, so it forms least similar to barium compound.
Hello!
Based on these facts, we should classify Germanium as a Metalloid.
Metalloids are chemical elements with a mixture of properties from metals and non-metals. Although Germanium has a metallic appearance (typical of metals), it doesn't have the conductive properties of metals, but is a semiconductor. The semiconductive properties of Germanium are used in applications like transistors and chips.
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