Answer:
ooh sorry, but will this help you now:
Ocean dynamics define and describe the motion of water within the oceans. Ocean temperature and motion fields can be separated into three distinct layers: mixed (surface) layer, upper ocean (above the thermocline), and deep ocean. Ocean currents are measured in sverdrup (sv), where 1 sv is equivalent to a volume flow rate of 1,000,000 m (35,000,000 cu ft) per second.
Surface currents, which make up only 8% of all water in the ocean, are generally restricted to the upper 4…
Explanation:
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Answer:
1.089%
Explanation:
From;
ν =1/2πc(k/meff)^1/2
Where;
ν = wave number
meff = reduced mass or effective mass
k = force constant
c= speed of light
Let
ν =1/2πc (k/meff)^1/2 vibrational wave number for 23Na35 Cl
ν' =1/2πc(k'/m'eff)^1/2 vibrational wave number for 23Na37 Cl
The between the two is obtained from;
ν' - ν /ν = (k'/m'eff)^1/2 - (k/meff)^1/2 / (k/meff)^1/2
Therefore;
ν' - ν /ν = [meff/m'eff]^1/2 - 1
Substituting values, we have;
ν' - ν /ν = [(22.9898 * 34.9688/22.9898 + 34.9688) * (22.9898 + 36.9651/22.9898 * 36.9651)]^1/2 -1
ν' - ν /ν = -0.01089
percentage difference in the fundamental vibrational wavenumbers of 23Na35Cl and 23Na37Cl;
ν' - ν /ν * 100
|(-0.01089)| × 100 = 1.089%
Answer:
Conduction, Convection and Radiation
Explanation:
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.
