What would substitution reaction looks like compairing to an
elimination reaction is GC analysis? And what...
What would substitution reaction looks like compairing to an
elimination reaction is GC analysis? And what are the possible
reasons that we might not see substitution in the GC analysis but
only see Elimination reaction.
Which of the following reaction conditions will increase the
ratio of substitution to elimination products in a reaction of an
alkyl halide?
a. Primary alkyl halide
b. Tertiary alkyl halide
c. Aqueous solution
d. High heat
e. Low heat
Solve the system using either Gaussian elimination with
back-substitution or Gauss-Jordan elimination. (If there is no
solution, enter NO SOLUTION. If the system has an infinite number
of solutions, express x, y, z, and
w in terms of the parameters t and
s.)
4x
+
12y
−
7z
−
20w
=
20
3x
+
9y
−
5z
−
28w
=
36
(x, y, z, w) = ( )
*Last person who solved this got it wrong
1. What would the Ns curve look like if the substitution effect
= income effect? Explain your answer.
2. Derive the Ys curve in the classical model.
3.. Derive the Yd curve in the classical model.
What it Looks Like to the User
The program will loop, asking the user for a bet amount from 0
to 100 (assume dollars, you can use ints or
longs). If the user types a 0 that means she wants
to quit. Otherwise, accept the amount as their bet and simulate a
slot machine pull. Your program will
print out a line that looks like a slot machine result containing
three strings. Some examples are: BAR 7 BAR, 7 7
cherries,...
Explain what the difference is between the alkyl substitution
reactions and addition/elimination type reactions in EAS
(electrophilic aromatic substitution).
describe the substitution method and the elimination
method of solving a system of equations. do they always give the
same answers? what is the difference between the methods?
Give the substitution and elimination products you would except
from the following reactions
(a)3-bromo-3-ethylpentane heated in methanol
(b) 1-iodo-1-methylcyclopentane heated in ethanol
(c) 3-bromo-2,2-dimethylbutane heated in ethanol