CHEM 250 Study Guide - Midterm Guide: Xylene, Boiling Point, Benzene

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31 May 2020
Department
Course
Professor
Chapter
13
alkane
:
hydrocarbons
where
each
carbon
atom
is
bonded
to
four
other
atoms
and
all
carbon
bonds
are
single
bonds
D-
alkenes
:
hydrocarbons
that
contain
a
carbon
-
carbon
double
bond
alkynes
:
hydrocarbons
that
contain
a
carbon
-
carbon
triple
bond
#
aromatic
:
hydrocarbons
that
have
one
or
more
benzene
-
like
rings
unsaturated
:
double
or
triple
carbon
-
carbon
bonds
saturated
:
only
single
carbon
-
carbon
bonds
n
beanf.ee?eha,szbo:ndinguT
o
(
ortho
)
1,2
di
-
substitution
m
(
meta
)
1,3
di
-
substitution
p
(
para
)
1,4
di
-
substitution
OH
÷
:÷÷¥::÷
.
:o÷
CH
3
o÷÷
:
"¥÷÷o÷
:
"o÷÷÷÷o÷
.
p
-
xylene
'
¥
.
¥÷
?
13503
H
=
sulfonic
acid
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13.3J
Benzene
Lewis
No
reactions
on
Exam
phenol
:
has
a
hydroxyl
group
directly
bonded
to
a
carbon
atom
of
a
benzene
ring
OH
acid
-
base
reaction
acid
(
phenol
)
+
base
salt-water
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Document Summary

Chapter 13 alkane : hydrocarbons where each carbon atom is bonded to four other atoms and all carbon bonds are single bonds. Benzene lewis phenol : has a hydroxyl group directly bonded to a carbon atom of a benzene ring. Oh acid - base reaction (cid:8869) acid (phenol) + base salt-water. , retain the finale in the name of the parent alkane (cid:8869) change the ending of the parent alkane from e to ol , and use a number to show the location of the -oh group. Substituents appear first in the name in alphabetical order with their positions given by the number of the carbon atom to which they are attached. 14. 2 e (cid:8869) boiling point = longer chain with -oh. Boiling points increase as intermolecular attractive forces increase. Solubility = shorter chain with - oh. Diol ending 2 higher molecular weight = higher boiling point higher solubility = lower molecular weight.

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