Estimate Δ S for the process depicted in Figure 17.1(a). if the apparatus contained 20 molecules in the flask on the left in the initial distribution, and each flask contained 10 molecules in the final distribution. Useful information: The number of ways to distribute n objects between two bins such that r particles are in one bin is called the number of combinations ( C ) and is given by the equation C ( n , r ) = n ! r ! ( n − r ) ! Where n ! (“ n factorial”) = 1 × 2 × 3 × … × n , and o! is defined to be 1.
Estimate Δ S for the process depicted in Figure 17.1(a). if the apparatus contained 20 molecules in the flask on the left in the initial distribution, and each flask contained 10 molecules in the final distribution. Useful information: The number of ways to distribute n objects between two bins such that r particles are in one bin is called the number of combinations ( C ) and is given by the equation C ( n , r ) = n ! r ! ( n − r ) ! Where n ! (“ n factorial”) = 1 × 2 × 3 × … × n , and o! is defined to be 1.
Solution Summary: The author explains the entropy of a spontaneous process, which is associated with the decrease in free energy in the system.
Estimate ΔS for the process depicted in Figure 17.1(a). if the apparatus contained 20 molecules in the flask on the left in the initial distribution, and each flask contained 10 molecules in the final distribution. Useful information: The number of ways to distribute n objects between two bins such that r particles are in one bin is called the number of combinations (C) and is given by the equation
C
(
n
,
r
)
=
n
!
r
!
(
n
−
r
)
!
Where n! (“n factorial”) = 1 × 2 × 3 × … × n, and o! is defined to be 1.
Using the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.
Synthesis of Dibenzalacetone
[References]
Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below.
Question 1
1 pt
Question 2
1 pt
Question 3
1 pt
H
Question 4
1 pt
Question 5
1 pt
Question 6
1 pt
Question 7
1pt
Question 8
1 pt
Progress:
7/8 items
Que Feb 24 at
You do not have to consider stereochemistry.
. Draw the enolate ion in its carbanion form.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
⚫ Separate multiple reactants using the + sign from the drop-down menu.
?
4
Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
The Laws of Thermodynamics, Entropy, and Gibbs Free Energy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=8N1BxHgsoOw;License: Standard YouTube License, CC-BY