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:
both are same give different number
Answer: 1090°C
Explanation: According to combined gas laws
(P1 × V1) ÷ T1 = (P2 × V2) ÷ T2
where P1 = initial pressure of gas = 80.0 kPa
V1 = initial volume of gas = 10.0 L
T1 = initial temperature of gas = 240 °C = (240 + 273) K = 513 K
P2 = final pressure of gas = 107 kPa
V2 = final volume of gas = 20.0 L
T2 = final temperature of gas
Substituting the values,
(80.0 kPa × 10.0 L) ÷ (513 K) = (107 kPa × 20.0 L) ÷ T2
T2 = 513 K × (107 kPa ÷80.0 kPa) × (20.0 L ÷ 10.0 L)
T2 = 513 K × (1.3375) × (2)
T2 = 1372.275 K
T2 = (1372.275 - 273) °C
T2 = 1099 °C
When you understand how neural pathways<span> are created in the brain, you ... But because I had the </span>will<span> to do it, I built a </span>new<span> pathway, and I rewired or reprogrammed my brain. ... can learn </span>new<span> behaviors and attitudes and can </span>transform<span> their </span>lives<span>. ... to the habit, and see what results you're </span>creating<span> in your </span><span>life</span>
Evaporation is the change from a liquid to gas