Part I: Hydrocarbon Structures and Names. INSTRUCTIONS: For each row in the table, you are given one of these four items: the line bond Hydrocarbon Structure Activity structure, the condensed structure, the skeletal structure, or the molecule's name. Use the given information to fill-in the other three items in the row. For the cyclic compound (fourth row), draw a side-view instead of a skeletal structure. LINE BOND STRUCTURE H -C-H. 1 1 A-C-C-C-C-C-G-H ITII1 HHHHHH H₂ H H 4 HICK=(IC-C-H 14 4 ### |H-C-C=C-C-C - H 1 H H H F-L H # HICIH H H 1 1 1 14 H HHH H HH 2c2c- VII HIGIHHI н-с CIH # F1 4 HIGIHITI I H H Η H T 1cc-H HI-= = HH HIC-CICIH H CONDENSED STRUCTURE CH3 CH3 CH₂CH-CH₂-Cit-CH₂-CH CH3-CEC-CH₂-CH3 CH=C H нас 1₂ CH₂ H 3CH₂CH3 H -CH3 C-H ICH3 CH₂CH3 1 CH3-CH₂-CH-CH-CH₂-CH₂-CH₂-CH₂ CH₂-CH₂-CH₂ SKELETAL STRUCTURE s I have added dots to indicate the position of carbon atoms Draw the side-view N NAME 2,4-dimethylhexane 2-pentyne trans-2-pentyne trans-1,2- dimethylcyclopentane 3-ethyl- 14-propyl- octane

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Chapter22: Organic And Biological Molecules
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Part I: Hydrocarbon Structures and Names. INSTRUCTIONS: For each row in the table, you are given one of these four items: the line bond
Hydrocarbon Structure Activity
structure, the condensed structure, the skeletal structure, or the molecule's name. Use the given information to fill-in the other three items in the row.
For the cyclic compound (fourth row), draw a side-view instead of a skeletal structure.
LINE BOND STRUCTURE
H
1
14-C-C-C
H
H
HIGH
H
コーヒーロー
11 1 11
АНАН Н
H
H-C-C=C-Ć-C-H
14 4
HHH
|H-C-C=C-C-C-H
H
| !!
H
#-L
++
#
H
H
--C- с
1
CICIG-H
T
H
H
Zc2c
1
H
HHH
1
T
H
H.
H
1
1
H
H H
I
H
H
I
C-H
±
H
H
HH
bclc c -H
H H
C
II
I
H H H H
H H
1 T
C -C
T
H
T
H
H
CONDENSED STRUCTURE
CH3
CH3
CH₂CH-CH₂-CH-CH₂-CH₂
CH3-CEC-CH₂-CH3
CH3
CH=CH
Η
C
1₂
CH₂
3CH₂CH
-CH3
-C-H
SKELETAL STRUCTURE
CH₂CH3
CH3-CH₂-CH-CH-CH₂-CH₂-CH₂-CH₂
CH₂-CH₂-CH₂
w
I have added dots to indicate the
position of carbon atoms
Draw the side-view
NAME
2,4-dimethylhexane
2-pentyne
trans-2-pentyne
trans-1,2-
dimethylcyclopentane
3-ethyl-
4-propyl-
octane
Transcribed Image Text:Part I: Hydrocarbon Structures and Names. INSTRUCTIONS: For each row in the table, you are given one of these four items: the line bond Hydrocarbon Structure Activity structure, the condensed structure, the skeletal structure, or the molecule's name. Use the given information to fill-in the other three items in the row. For the cyclic compound (fourth row), draw a side-view instead of a skeletal structure. LINE BOND STRUCTURE H 1 14-C-C-C H H HIGH H コーヒーロー 11 1 11 АНАН Н H H-C-C=C-Ć-C-H 14 4 HHH |H-C-C=C-C-C-H H | !! H #-L ++ # H H --C- с 1 CICIG-H T H H Zc2c 1 H HHH 1 T H H. H 1 1 H H H I H H I C-H ± H H HH bclc c -H H H C II I H H H H H H 1 T C -C T H T H H CONDENSED STRUCTURE CH3 CH3 CH₂CH-CH₂-CH-CH₂-CH₂ CH3-CEC-CH₂-CH3 CH3 CH=CH Η C 1₂ CH₂ 3CH₂CH -CH3 -C-H SKELETAL STRUCTURE CH₂CH3 CH3-CH₂-CH-CH-CH₂-CH₂-CH₂-CH₂ CH₂-CH₂-CH₂ w I have added dots to indicate the position of carbon atoms Draw the side-view NAME 2,4-dimethylhexane 2-pentyne trans-2-pentyne trans-1,2- dimethylcyclopentane 3-ethyl- 4-propyl- octane
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