The following observations were made for a series of five oil drops an experiment similar to Millikan's (see Figure 2-8). Drop 1 carried acharge of 1.28 × 10 − 18 C drops 2 and 3 each carried 1 2 the charge of drop 1; drop 4 carried 1 8 the charge of drop 1; drop 5 had a charge four times that of drop 1. Are these data consistent with the value of the electronic charge given in the text? Could Millikan have inferred the charge on the electron from this particular series of data? Explain.
The following observations were made for a series of five oil drops an experiment similar to Millikan's (see Figure 2-8). Drop 1 carried acharge of 1.28 × 10 − 18 C drops 2 and 3 each carried 1 2 the charge of drop 1; drop 4 carried 1 8 the charge of drop 1; drop 5 had a charge four times that of drop 1. Are these data consistent with the value of the electronic charge given in the text? Could Millikan have inferred the charge on the electron from this particular series of data? Explain.
Solution Summary: The author explains the inferred possibility of the charge on the electron from Millikan's oil-drop experiment.
The following observations were made for a series of five oil drops an experiment similar to Millikan's (see Figure 2-8). Drop 1 carried acharge of
1.28
×
10
−
18
C drops 2 and 3 each carried
1
2
the charge of drop 1; drop 4 carried
1
8
the charge of drop 1; drop 5 had a charge four times that of drop 1. Are these data consistent with the value of the electronic charge given in the text? Could Millikan have inferred the charge on the electron from this particular series of data? Explain.
Q1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for
each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and
B? How about the diastereomers (A versus C or B versus C)?
H Br
H Br
(S) CH3
(R) CH3
H3C (S)
H3C
H Br
Br
H
A
C
enantiomers
H Br
H Br
(R) CH3
H3C (R)
(S) CH3
H3C
H Br
Br H
B
D
identical
2. Histamine (below structure) is a signal molecule involved in immune response and is
a neurotransmitter. Histamine features imidazole ring which is an aromatic heterocycle.
Please answer the following questions regarding Histamine.
b
a
HN
=N
C
NH2
a. Determine hybridization of each N atom (s, p, sp, sp², sp³, etc.) in histamine
N-a hybridization:
N-b hybridization:
N-c hybridization:
b. Determine what atomic orbitals (s, p, sp, sp², sp³, etc.) of the lone pair of each N
atom resided in
N-a hybridization:
N-b hybridization:
N-c hybridization:
Chapter 2 Solutions
General Chemistry: Principles And Modern Applications Plus Mastering Chemistry With Pearson Etext -- Access Card Package (11th Edition)
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