(a)
Interpretation:
Structural formula for the given
Concept Introduction:
Structure of the aldehyde can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an aldehyde the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- • Expanded structural formula
- • Condensed structural formula
- • Skeletal structural formula
- • Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(a)
Answer to Problem 15.21EP
The structural formula for 3-methylpentanal is,
Explanation of Solution
The given name of the compound is 3-methylpentanal. From the name it is understood that the parent carbon chain is pentane and it contains five carbon atoms. The parent chain can be drawn as shown below,
From the name of the given aldehyde, the substituents that are present can be identified. In this case, the substituent is a methyl group on third carbon atom. The first carbon atom has to be the carbonyl carbon atom as the given compound is an aldehyde.
Carbon atom has a valence of four. Hence, carbon atom can form four covalent bonds. The remaining bonds are satisfied by hydrogen atom. The structure is obtained as shown below,
Structural formula for the given aldehyde is drawn.
(b)
Interpretation:
Structural formula for the given aldehyde has to be drawn.
Concept Introduction:
Structure of the aldehyde can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an aldehyde the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- • Expanded structural formula
- • Condensed structural formula
- • Skeletal structural formula
- • Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(b)
Answer to Problem 15.21EP
The structural formula for 2-ethylhexanal is,
Explanation of Solution
The given name of the compound is 2-ethylhexanal. From the name it is understood that the parent carbon chain is hexane and it contains six carbon atoms. The parent chain can be drawn as shown below,
From the name of the given aldehyde, the substituents that are present can be identified. In this case, the substituent is an ethyl group on second carbon atom. The first carbon atom has to be the carbonyl carbon atom as the given compound is an aldehyde.
Carbon atom has a valence of four. Hence, carbon atom can form four covalent bonds. The remaining bonds are satisfied by hydrogen atom. The structure is obtained as shown below,
Structural formula for the given aldehyde is drawn.
(c)
Interpretation:
Structural formula for the given aldehyde has to be drawn.
Concept Introduction:
Structure of the aldehyde can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an aldehyde the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- • Expanded structural formula
- • Condensed structural formula
- • Skeletal structural formula
- • Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(c)
Answer to Problem 15.21EP
The structural formula for 2,2-dichloropropanal is,
Explanation of Solution
The given name of the compound is 2,2-dichloropropanal. From the name it is understood that the parent carbon chain is propane and it contains three carbon atoms. The parent chain can be drawn as shown below,
From the name of the given aldehyde, the substituents that are present can be identified. In this case, the substituents are two chlorine atoms on second carbon atom. The first carbon atom has to be the carbonyl carbon atom as the given compound is an aldehyde.
Carbon atom has a valence of four. Hence, carbon atom can form four covalent bonds. The remaining bonds are satisfied by hydrogen atom. The structure is obtained as shown below,
Structural formula for the given aldehyde is drawn.
(d)
Interpretation:
Structural formula for the given aldehyde has to be drawn.
Concept Introduction:
Structure of the aldehyde can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an aldehyde the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- • Expanded structural formula
- • Condensed structural formula
- • Skeletal structural formula
- • Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(d)
Answer to Problem 15.21EP
The structural formula for 4-hydroxy-2-methyloctanal is,
Explanation of Solution
The given name of the compound is 4-hydroxy-2-methyloctanal. From the name it is understood that the parent carbon chain is octane and it contains eight carbon atoms. The parent chain can be drawn as shown below,
From the name of the given aldehyde, the substituents that are present can be identified. In this case, the substituents are a methyl group on second carbon atom and a hydroxyl group on fourth carbon atom. The first carbon atom has to be the carbonyl carbon atom as the given compound is an aldehyde.
Carbon atom has a valence of four. Hence, carbon atom can form four covalent bonds. The remaining bonds are satisfied by hydrogen atom. The structure is obtained as shown below,
Structural formula for the given aldehyde is drawn.
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Chapter 15 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- Determine if the following salt is neutral, acidic or basic. If acidic or basic, write the appropriate equilibrium equation for the acid or base that exists when the salt is dissolved in aqueous solution. If neutral, simply write only NR. Be sure to include the proper phases for all species within the reaction LiNO3arrow_forwardAn unknown weak acid with a concentration of 0.410 M has a pH of 5.600. What is the Ka of the weak acid?arrow_forward(racemic) 19.84 Using your reaction roadmaps as a guide, show how to convert 2-oxepanone and ethanol into 1-cyclopentenecarbaldehyde. You must use 2-oxepanone as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way. & + EtOH H 2-Oxepanone 1-Cyclopentenecarbaldehydearrow_forward
- R₂ R₁ R₁ a R Rg Nu R₂ Rg R₁ R R₁₂ R3 R R Nu enolate forming R₁ R B-Alkylated carbonyl species or amines Cyclic B-Ketoester R₁₁ HOB R R₁B R R₁₂ B-Hydroxy carbonyl R diester R2 R3 R₁ RB OR R₂ 0 aB-Unsaturated carbonyl NaOR Aldol HOR reaction 1) LDA 2) R-X 3) H₂O/H₂O ketone, aldehyde 1) 2°-amine 2) acid chloride 3) H₂O'/H₂O 0 O R₁ R₁ R R₁ R₁₂ Alkylated a-carbon R₁ H.C R₁ H.C Alkylated methyl ketone acetoacetic ester B-Ketoester ester R₁ HO R₂ R B-Dicarbonyl HO Alkylated carboxylic acid malonic ester Write the reagents required to bring about each reaction next to the arrows shown. Next, record any regiochemistry or stereochemistry considerations relevant to the reaction. You should also record any key aspects of the mechanism, such as forma- tion of an important intermediate, as a helpful reminder. You may want to keep track of all reactions that make carbon-carbon bonds, because these help you build large molecules from smaller fragments. This especially applies to the reactions in…arrow_forwardProvide the reasonable steps to achieve the following synthesis.arrow_forwardIdentify which compound is more acidic. Justify your choice.arrow_forward
- Provide the reasonable steps to achieve the following synthesis.arrow_forwardWhen anisole is treated with excess bromine, the reaction gives a product which shows two singlets in 1H NMR. Draw the product.arrow_forward(ii) Draw a reasonable mechanism for the following reaction: CI NaOH heat OH (hint: SNAr Reaction) :arrow_forward
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