The validation about the presence of a “head and two tails” structure in the given substance has to be predicted. Concept introduction: The “head and two tails” model gives the orientation of groups in space. It has two parts, the head which is polar and the two tails, which are non-polar. The polar part of the model is soluble in water, so it is hydrophilic in nature. The non-polar part of the model is insoluble in water, so it is hydrophobic in nature.
The validation about the presence of a “head and two tails” structure in the given substance has to be predicted. Concept introduction: The “head and two tails” model gives the orientation of groups in space. It has two parts, the head which is polar and the two tails, which are non-polar. The polar part of the model is soluble in water, so it is hydrophilic in nature. The non-polar part of the model is insoluble in water, so it is hydrophobic in nature.
Solution Summary: The author explains that the "head and two tails" model gives the orientation of groups in space. The 18 carbon monounsaturated amino dialcohol platform for sphingophospholipids.
Definition Definition Simplest organic compounds that contain only single bonds between carbon – carbon atoms and carbon – hydrogen bonds. This means they are a series of saturated compounds with a general molecular formula, C n H 2n+2 .
Chapter 8, Problem 8.156EP
(a)
Interpretation Introduction
Interpretation: The validation about the presence of a “head and two tails” structure in the given substance has to be predicted.
Concept introduction: The “head and two tails” model gives the orientation of groups in space. It has two parts, the head which is polar and the two tails, which are non-polar. The polar part of the model is soluble in water, so it is hydrophilic in nature. The non-polar part of the model is insoluble in water, so it is hydrophobic in nature.
(b)
Interpretation Introduction
Interpretation: The validation about the presence of a “head and two tails” structure in the given substance has to be predicted.
Concept introduction: The “head and two tails” model gives the orientation of groups in space. It has two parts, the head which is polar and the two tails, which are non-polar. The polar part of the model is soluble in water, so it is hydrophilic in nature. The non-polar part of the model is insoluble in water, so it is hydrophobic in nature.
(c)
Interpretation Introduction
Interpretation: The validation about the presence of a “head and two tails” structure in the given substance has to be predicted.
Concept introduction: The “head and two tails” model gives the orientation of groups in space. It has two parts, the head which is polar and the two tails, which are non-polar. The polar part of the model is soluble in water, so it is hydrophilic in nature. The non-polar part of the model is insoluble in water, so it is hydrophobic in nature.
(d)
Interpretation Introduction
Interpretation: The validation about the presence of a “head and two tails” structure in the given substance has to be predicted.
Concept introduction: The “head and two tails” model gives the orientation of groups in space. It has two parts, the head which is polar and the two tails, which are non-polar. The polar part of the model is soluble in water, so it is hydrophilic in nature. The non-polar part of the model is insoluble in water, so it is hydrophobic in nature.
Q3: Describes the relationship (identical, constitutional isomers, enantiomers or diastereomers)
of each pair of compounds below.
ག
H
CH3
OH
OH
CH3
H3C
OH
OH
OH
//////////
C
CH3
CH3
CH3
CH3
H3C
CH 3
C/III.....
Physics & Astronomy
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COOH
H
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H
2
OH
HO
CH3
HOOC
H
CH3
CH3
CH3
Br.
H
H
Br
and
H
H
H
H
Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label
each compound as chiral or achiral.
OH
HO
CI
Br
H
CI
CI
Br
CI
CI
Xf x f g
Br
D
OH
Br
Br
H₂N
R.
IN
Ill
I
-N
S
OMe
D
II
H
CO₂H
1/111
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These are synthesis questions. You need to show how the starting material can be converted into
the product(s) shown. You may use any reactions we have learned. Show all the reagents you
need. Show each molecule synthesized along the way and be sure to pay attention to the
regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made
along the way, you need to draw both enantiomers and label the mixture as "racemic".
All of the carbon atoms of the products must come from the starting material!
?
H
H
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