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(a)
Interpretation:
Structural formula for the given
Concept Introduction:
Structure of the given 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)
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Answer to Problem 4.25EP
The structural formula for formaldehyde is,
Explanation of Solution
The given name of the compound is formaldehyde. From the name it is understood that the parent carbon chain is methane and it contains only one carbon atom. Two hydrogen atoms are attached to the carbonyl carbon atom. The structure of formaldehyde is given 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 given 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)
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Answer to Problem 4.25EP
The structural formula for propionaldehyde is,
Explanation of Solution
The given name of the compound is propionaldehyde. 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, there are no substitutents. 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 given 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)
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Answer to Problem 4.25EP
The structural formula for 2-chlorobenzaldehyde is,
Explanation of Solution
The given name of the compound is 2-chlorobenzaldehyde. From the name it is understood that the parent carbon chain is benzene ring. 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 chloro group in the 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 given 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)
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Answer to Problem 4.25EP
The structural formula for 2,4-dimethylbenzaldehyde is,
Explanation of Solution
The given name of the compound is 2,4-dimethylbenzaldehyde. From the name it is understood that the parent carbon chain is benzene ring. 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 methyl groups, each on second carbon atom and 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 4 Solutions
Organic And Biological Chemistry
- Nonearrow_forwardNonearrow_forwardman Campus Depa (a) Draw the three products (constitutional isomers) obtained when 2-methyl-3-hexene reacts with water and a trace of H2SO4. Hint: one product forms as the result of a 1,2-hydride shift. (1.5 pts) This is the acid-catalyzed alkene hydration reaction.arrow_forward
- (6 pts - 2 pts each part) Although we focused our discussion on hydrogen light emission, all elements have distinctive emission spectra. Sodium (Na) is famous for its spectrum being dominated by two yellow emission lines at 589.0 and 589.6 nm, respectively. These lines result from electrons relaxing to the 3s subshell. a. What is the photon energy (in J) for one of these emission lines? Show your work. b. To what electronic transition in hydrogen is this photon energy closest to? Justify your answer-you shouldn't need to do numerical calculations. c. Consider the 3s subshell energy for Na - use 0 eV as the reference point for n=∞. What is the energy of the subshell that the electron relaxes from? Choose the same emission line that you did for part (a) and show your work.arrow_forwardNonearrow_forward(9 Pts) In one of the two Rare Earth element rows of the periodic table, identify an exception to the general ionization energy (IE) trend. For the two elements involved, answer the following questions. Be sure to cite sources for all physical data that you use. a. (2 pts) Identify the two elements and write their electronic configurations. b. (2 pts) Based on their configurations, propose a reason for the IE trend exception. c. (5 pts) Calculate effective nuclear charges for the last electron in each element and the Allred-Rochow electronegativity values for the two elements. Can any of these values explain the IE trend exception? Explain how (not) - include a description of how IE relates to electronegativity.arrow_forward
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