1-Octene-3-ol can be prepared from hexanal in two steps. The first step involves an actylide addition reaction to hexanal. The structure of the product formed in this step is to be given and how to convert it in to 1-octene-3-ol is also to be stated. Concept introduction: When aldehydes and ketones are treated with sodium acetylide in the presence of dilute acids addition reaction occurs. The acetylide ion adds to the carbonyl carbon of the aldehyde and H adds to the carbonyl oxygen to yield an ynol in which the alcohol group is adjacent to a carbon in triple bond. To give: The structure of the product formed in the step during the reaction between hexanal and sodium acetylide in the presence of dilute acids and further to state how it can be converted in to 1-octene-3-ol.

Question

Draw all resonance structures for the following ion: CH₂ Draw all resonance structures on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. 2D ד CONT HD EXP CON ? 1 [1] Α 12 Marvin JS by Chemaxon A DOO H C N Br I UZ OSPF

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 9.SE, Problem 52AP

Interpretation Introduction

Interpretation:

1-Octene-3-ol can be prepared from hexanal in two steps. The first step involves an actylide addition reaction to hexanal. The structure of the product formed in this step is to be given and how to convert it in to 1-octene-3-ol is also to be stated.

Concept introduction:

When aldehydes and ketones are treated with sodium acetylide in the presence of dilute acids addition reaction occurs. The acetylide ion adds to the carbonyl carbon of the aldehyde and H adds to the carbonyl oxygen to yield an ynol in which the alcohol group is adjacent to a carbon in triple bond.

To give:

The structure of the product formed in the step during the reaction between hexanal and sodium acetylide in the presence of dilute acids and further to state how it can be converted in to 1-octene-3-ol.

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Draw all resonance structures for the following ion: CH₂ Draw all resonance structures on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. 2D ד CONT HD EXP CON ? 1 [1] Α 12 Marvin JS by Chemaxon A DOO H C N Br I UZ OSPF

What is the average mass of the 10 pennies? Report your value with correct significant figures. What is the error (uncertainty) associated with each mass measurement due to the equipment? What is the uncertainty associated with the average value? Note that the uncertainty of the balance will propagate throughout the calculation. What is the standard deviation of the 10 mass measurements? Explain the difference between the propagated uncertainty and the standard deviation. Which number would you use to describe the uncertainty in the measurement? Calculate the total mass of the pennies with associated uncertainty. Calculate the average density of a penny based on these data. Propagate the uncertainty values for both mass and volume in your calculations.

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Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 9.SE, Problem 52AP

Interpretation Introduction

Interpretation:

1-Octene-3-ol can be prepared from hexanal in two steps. The first step involves an actylide addition reaction to hexanal. The structure of the product formed in this step is to be given and how to convert it in to 1-octene-3-ol is also to be stated.

Concept introduction:

When aldehydes and ketones are treated with sodium acetylide in the presence of dilute acids addition reaction occurs. The acetylide ion adds to the carbonyl carbon of the aldehyde and H adds to the carbonyl oxygen to yield an ynol in which the alcohol group is adjacent to a carbon in triple bond.

To give:

The structure of the product formed in the step during the reaction between hexanal and sodium acetylide in the presence of dilute acids and further to state how it can be converted in to 1-octene-3-ol.

Expert Solution & Answer

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Check out sample textbook solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 9.SE, Problem 52AP

Interpretation Introduction

Interpretation:

1-Octene-3-ol can be prepared from hexanal in two steps. The first step involves an actylide addition reaction to hexanal. The structure of the product formed in this step is to be given and how to convert it in to 1-octene-3-ol is also to be stated.

Concept introduction:

When aldehydes and ketones are treated with sodium acetylide in the presence of dilute acids addition reaction occurs. The acetylide ion adds to the carbonyl carbon of the aldehyde and H adds to the carbonyl oxygen to yield an ynol in which the alcohol group is adjacent to a carbon in triple bond.

To give:

The structure of the product formed in the step during the reaction between hexanal and sodium acetylide in the presence of dilute acids and further to state how it can be converted in to 1-octene-3-ol.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 9.SE, Problem 52AP

Interpretation Introduction