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:
1.5 M.
Explanation:
- Molarity (M) is defined as the no. of moles of solute dissolved in a 1.0 L of the solution.
<em>M = (no. of moles of LiBr)/(Volume of the solution (L).</em>
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∵ no. of moles of LiBr = (mass/molar mass) of LiBr = (97.7 g)/(86.845 g/mol) = 1.125 mol.
Volume of the solution = 750.0 mL = 0.75 L.
∴ M = (no. of moles of luminol)/(Volume of the solution (L) = (1.125 mol)/(0.75 L) = 1.5 M.
<span>Carbon dioxide CO2 and water H2O. Through photosynthesis makes sugar C6H12O6.</span>
Contains DNA, contains ribosomes, lacks a nucleus
Answer:
Gravity always pulls objects such as a desk, book or person down. Thus, when you jump gravity causes you to land on the ground. Friction, however, doesn't pull objects down
