Find out how much the donuts cost then divide that by $10,000 and you will get your answer
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.
Molar mass ethanol:
C2H5OH = 12 x 2+ 1 x 5 + 16 + 1 = 46.0 g/mol
volume = 545 mL in liters: 545 / 1000 => 0.545 L
number of moles:
29.0 / 46.0 => 0.6304 moles
M = n / V
M = 0.6304 / 0.545
M = 1.156 mol/L
hope this helps!
This is called the pedigree chart.
Answer:
Change in internal energy (ΔU) = -9 KJ
Explanation:
Given:
q = –8 kJ [Heat removed]
w = –1 kJ [Work done]
Find:
Change in internal energy (ΔU)
Computation:
Change in internal energy (ΔU) = q + w
Change in internal energy (ΔU) = -8 KJ + (-1 KJ)
Change in internal energy (ΔU) = -8 KJ - 1 KJ
Change in internal energy (ΔU) = -9 KJ
