a.True.
The ordely geometric arrangement of atmos is called a crystalline solid.
Answer:
2-ethoxy-2-methylpropan-1-ol
Explanation:
On this reaction, we have an "<u>epoxide"</u> (2-methyl-1,2-epoxypropane). Additionally, we have <u>acid medium</u> (due to the sulfuric acid
). The acid medium will produce the <u>hydronium ion</u> (
). This ion would be attacked by the oxygen of the epoxide. Then a <u>carbocation</u> would be produced, in this case, the most stable carbocation is the <u>tertiary one</u>. Then an <u>ethanol</u> molecule acts as a nucleophile and will attack the carbocation. Finally, a <u>deprotonation </u>step takes place to produce <u>2-ethoxy-2-methylpropan-1-ol</u>.
See figure 1
I hope it helps!
Height of wave - amplitude
Higher the pitch - higher the frequency
Louder - higher the amplitude
bottom of the wave - trough
distance from crest to crest - wave length
top of the wave - crest
Answer:
Yes
Explanation:
Isotopes are atoms of the same element that have different numbers of neutrons in their nuclei. Everything else about them is the same.(If you want more explanation tell me).
Answer:
a) IUPAC Names:
1) (<em>trans</em>)-but-2-ene
2) (<em>cis</em>)-but-2-ene
3) but-1-ene
b) Balance Equation:
C₄H₁₀O + H₃PO₄ → C₄H₈ + H₂O + H₃PO₄
As H₃PO₄ is catalyst and remains unchanged so we can also write as,
C₄H₁₀O → C₄H₈ + H₂O
c) Rule:
When more than one alkene products are possible then the one thermodynamically stable is favored. Thermodynamically more substituted alkenes are stable. Furthermore, trans alkenes are more stable than cis alkenes. Hence, in our case the major product is trans alkene followed by cis. The minor alkene is the 1-butene as it is less substituted.
d) C is not Geometrical Isomer:
For any alkene to demonstrate geometrical isomerism it is important that there must be two different geminal substituents attached to both carbon atoms. In 1-butene one carbon has same geminal substituents (i.e H atoms). Hence, it can not give geometrical isomers.