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:
0.681 atm
Explanation:
To solve this problem, we make use of the General gas equation.
Given:
P1 = 785 torr
V1 = 2L
T1 = 37= 37 + 273.15 = 310.15K
P2 = ?
V2 = 3.24L
T2 = 58 = 58+273.15 = 331.15K
P1V1/T1 = P2V2/T2
Now, making P2 the subject of the formula,
P2 = P1V1T2/T1V2
P2 = [785 * 2 * 331.15]/[310.15 * 3.24]
P2 = 515.715 Torr
We convert this to atm: 1 torr = 0.00132 atm
515.715 Torr = 515.715 * 0.00132 = 0.681 atm
Heat radiates from the fire and cooks the marshmallow because heat transfer.
Answer:
The advantage of this technique is that purified water as well as deposited metals can be re-used. It is necessary to use an inert electrode, such as platinum, because there is no metal present to conduct the electrons from the anode to the cathode.
