Answer:
Explanation:
An electron-donating heteroatom substituent at position-2 of a furan promotes regiospecific opening of the 7-oxa bridge of the Diels-Alder cycloadduct with hexafluoro-2-butyne, producing a 4-heterosubstituted 2,3-di(trifluoromethyl)phenol building block in a single step. The phenol and heteroatom substituent are easily transformed to the corresponding iodide or triflate that readily undergoes Heck, Suzuki, and Stille reactions to install a variety of substituents in high yields. This methodology provides a facile and general synthesis of 1,4-disubsituted 2, 3-di(trifluoromethyl)benzenes.
M = 4 g = 4/1000 kg = 0.004 kg, θ₂ = 21.0°C, θ₁ = 0°C , c = 0.44kJ/kg°C,
Q = mc(θ₂ - θ₁)
Q = 0.004*0.440*(21 - 0)
Q = 0.03696 kJ
0.03696 kJ<span> of heat is absorbed.</span>
Ionization Trend: First ionization energy will increase left to right across a period and increase bottom to top of a family (column).
A) Sr, Be, Mg are all in column 2 of the periodic table. Based on the first ionization rule above, from increasing to decreasing energy, the order is: Be, Mg, Sr
B) Bi, Cs, Ba are all in the same row of the periodic table. Based on the first ionization rule above, from increasing to decreasing energy, the order is: Bi, Ba, Cs
C) Same rule as above. Order is: Na, Al, S
Is volume one of your answers?
