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(a)
Interpretation:
The compound 1-pentene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
(b)
Interpretation:
The compound 2-pentene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
(c)
Interpretation:
The compound 1-chloropropene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
(d)
Interpretation:
The compound 2-chloropropene exhibit geometric isomerism or not has to be given and two isomers has to be drawn and named for the given structure.
Concept Introduction:
The structure of the compound is given by its systematic name.
To give the structure from the name of the compound, the root name has to be identified. The root name indicates the number of carbon atoms present in the longest chain.
Then the functional group (suffix) has to be identified. It indicates whether any functional groups are present in the compound, it also gives whether the compound is an alkane or alkene or alkyne.
The prefix of the name indicates the branched groups and their positions on the carbon chain.
The name of the compound is in the form
Prefix + Root + Suffix
The geometric isomers are said to be the isomers which shows different orientation of groups around a double bond. The geometric isomers are also known as cis-trans isomers.
When two similar or higher priority groups are attached to the carbon on same side, it is said to be cis-isomer.
When two similar or higher priority groups are attached to the carbon on opposite sides, it is said to be trans-isomer.
To exhibit the geometric isomerism, a molecule should have double bonded carbon atoms (
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Chapter 15 Solutions
ALEKS 360 for Silberberg Chemistry: The Molecular Nature of Matter and Change
- Question 7 (10 points) Identify the carboxylic acid present in each of the following items and draw their structures: Food Vinegar Oranges Yogurt Sour Milk Pickles Acid Structure Paragraph ✓ BI UAE 0118 + v Task: 1. Identify the carboxylic acid 2. Provide Name 3. Draw structure 4. Take a picture of your table and insert Add a File Record Audio Record Video 11.arrow_forwardCheck the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 IZ IN Molecule 4 Molecule 5 ZI none of the above ☐ Molecule 3 Х IN www Molecule 6 NH Garrow_forwardHighlight each chiral center in the following molecule. If there are none, then check the box under the drawing area. There are no chiral centers. Cl Cl Highlightarrow_forward
- A student proposes the following two-step synthesis of an ether from an alcohol A: 1. strong base A 2. R Is the student's proposed synthesis likely to work? If you said the proposed synthesis would work, enter the chemical formula or common abbreviation for an appropriate strong base to use in Step 1: If you said the synthesis would work, draw the structure of an alcohol A, and the structure of the additional reagent R needed in Step 2, in the drawing area below. If there's more than one reasonable choice for a good reaction yield, you can draw any of them. ☐ Click and drag to start drawing a structure. Yes No ロ→ロ 0|0 G Х D : ☐ பarrow_forwardटे Predict the major products of this organic reaction. Be sure to use wedge and dash bonds when necessary, for example to distinguish between different major products. ☐ ☐ : ☐ + NaOH HO 2 Click and drag to start drawing a structure.arrow_forwardShown below are five NMR spectra for five different C6H10O2 compounds. For each spectrum, draw the structure of the compound, and assign the spectrum by labeling H's in your structure (or in a second drawing of the structure) with the chemical shifts of the corresponding signals (which can be estimated to nearest 0.1 ppm). IR information is also provided. As a reminder, a peak near 1700 cm-1 is consistent with the presence of a carbonyl (C=O), and a peak near 3300 cm-1 is consistent with the presence of an O–H. Extra information: For C6H10O2 , there must be either 2 double bonds, or 1 triple bond, or two rings to account for the unsaturation. There is no two rings for this problem. A strong band was observed in the IR at 1717 cm-1arrow_forward
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