From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn. Concept Introduction: Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted. Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon Predicting cis-trans isomers: In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like, Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side. Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Question

Want to see the full answer?

Answer 1

Question

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

carbons in each of the structures below. For instance, the central carbon of chloromethylbutane (pictured 3. A chiral carbon is a carbon that is single-bonded to four different types of groups. Identify the chiral above) is a chiral carbon. (Can you see how the groups attached to it are all chemically different?) In each of the chiral molecules below, identify all the carbons that are chiral carbons by drawing a circle around each one of them. (a) the carbohydrate glucose H O (b) the carbohydrate fructose CH₂OH 1C H-C-OH 3 HO-C-H 4 H-C-OH 5 H-C-OH 6CH₂OH D-Glucose (linear form) (c) the amino acid leucine O O H3C. HO H H- -OH CH 3 NH2 H- -OH CH₂OH OH

We always include controls in the Annexin-V-GFP/Propidium Iodide flow cytometric assay to study apoptosis. List four types of controls in this assay. Why do we need these controls? Explain your answers. After the flow assay, if we like to examine the morphology of the viable, early apoptotic and late apoptotic cells by confocal microscopy, what can we do and what are the expected results?

3. (2 points) Your lab partner accidentally used a pen instead of a pencil to mark the baseline and label the lanes of their TLC plate. Briefly (1-2 sentences for each point) describe (a) what would happen to the ink when you develop the TLC plate; and (b) how this would affect the experiment. 1

Answer 2

Question

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 6

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 7

Chapter 13.3, Problem 13.4P

(a)

Interpretation Introduction

Interpretation:

From the condensed structures for 2,3-dimethyl-2-pentene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Predicting cis-trans isomers:

In general, the alkene can exist as cis or trans isomer only if the two substituents on each carbon are not equal. Like,

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 8

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 9

(b)

Interpretation Introduction

Interpretation:

From the both condensed and line structures for 2-Methyl-2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 10

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 11

(c)

Interpretation Introduction

Interpretation:

From the line structures for 2-hexene whether cis-trans isomers exist or not has to be given. And if it exists, both the isomers has to be drawn.

Concept Introduction:

Condensed structures: A condensed structures only shows the total number of atoms but not bonds exist between the atoms. The vertical and horizontal line which represents bonding all should be omitted.

Line structure: In organic compounds, the series of atoms in the compound are bonded together which shown by drawing a line between them. End of line segment represents carbon

Cis-isomer: In cis-configuration, the two bulkier substituents of the double bond are on the same side.

Trans-isomer: In trans-configuration, the two bulkier substituents of the double bond are on the opposite side.

Answer 12

Expert Solution & Answer

Answer 13

Expert Solution & Answer

Answer 14

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 15

Ch. 13.2 - Prob. 13.1P Ch. 13.2 - Prob. 13.2P Ch. 13.2 - What are the IUPAC names of the two alkenes shown...Ch. 13.3 - Prob. 13.4P Ch. 13.3 - Prob. 13.5P Ch. 13.3 - Prob. 13.6KCP Ch. 13.5 - Prob. 13.7P Ch. 13.5 - Many biological transformations can be simply...Ch. 13.5 - (a) After the reaction of 11-cis-retinal with...Ch. 13.5 - Prob. 13.2CIAP

Solution Summary: The author explains how the condensed structures of 2,3-dimethyl-2-pentene show whether cis-trans isomers exist or not.

Concept explainers

Want to see the full answer?

Chapter 13 Solutions