
(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.
(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.
(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.
(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.

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Chapter 15 Solutions
General, Organic, and Biological Chemistry Seventh Edition
- Draw the structure of A, the minor E1 product of the reaction. Cl Skip Part Check F1 esc CH_CH OH, D 3 2 Click and drag to start drawing a structure. 80 R3 F4 F2 F3 @ 2 # $ 4 3 Q W 95 % KO 5 F6 A F7 × G ☐ Save For Later Sub 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy C ►II A A F8 F9 F10 FL 6 7 88 & * 8 9 LLI E R T Y U A S D lock LL F G H 0 P J K L Z X C V B N M 9 Harrow_forwardFrom the choices given, which two substances have the same crystal structure? (Select both) Group of answer choices ZnS (zincblende) Diamond TiO2 (rutile) ZnS (wurtzite)arrow_forwardPotassium (K) blends with germanium (Ge) to form a Zintl phase with a chemical formula of K4Ge4. Which of the following elements would you expect potassium to blend with to form an alloy? Electronegativities: As (2.0), Cl (3.0), Ge (1.8), K (0.8), S (2.5), Ti (1.5) Group of answer choices Arsenic (As) Sulfur (S) Chlorine (Cl) Titanium (Ti)arrow_forward
- Consider two elements, X and Z. Both have cubic-based unit cells with the same edge lengths. X has a bcc unit cell while Z has a fcc unit cell. Which of the following statements is TRUE? Group of answer choices Z has a larger density than X X has more particles in its unit cell than Z does X has a larger density than Z Z has a larger unit cell volume than Xarrow_forwardHow many particles does a face-centered cubic (fcc) unit cell contain? Group of answer choices 2 14 8 4arrow_forwardV Highlight all of the carbon atoms that have at least one beta (B) hydrogen, using red for one ẞ hydrogen, blue for two ẞ hydrogens, and green for three ẞ hydrogens. If none of the carbon atoms have ẞ hydrogens, check the box underneath the molecule. ED X None of the carbon atoms have ẞ hydrogens. Explanation esc 2 Check * F1 F2 1 2 80 # 3 Q W tab A caps lock shift fn control F3 N S option O 694 $ F4 F5 F6 005 % E R D F LL 6 olo 18 Ar B © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility A DII F7 F8 87 & * 8 T Y U G H 4 F9 F10 ( 9 0 E F11 F12 உ J K L + || X C V B N M H H command option commandarrow_forward
- Consider the reaction below and answer the following questions. Part 1 of 4 Br NaOCH2CH3 Identify the mechanisms involved. Check all that apply. SN 1 SN 2 E1 E2 None of the above Part 2 of 4 Skip Part Check esc F1 F2 lock 1 2 Q W A S #3 80 F3 F4 F5 F6 Save For © 2025 McGraw Hill LLC. All Rights Reserved. Terms ˇˇ % & 4 5 6 89 7 IK A 分 བ F7 F8 F9 F * E R T Y U 8 9 D F G H K V B N M 0 Oarrow_forwardWhat kind of holes are not generated when solid-state particles adopt a close packing pattern? Group of answer choices tetrahedral cubic octahedral None of the other choices are correctarrow_forwardFor the reaction below: 1. Draw all reasonable elimination products to the right of the arrow. 2. In the box below the reaction, redraw any product you expect to be a major product. 田 Major Product: Check ☐ + I Na OH esc F1 F2 2 1 @ 2 Q W tab A caps lock S #3 80 F3 69 4 σ F4 % 95 S Click and drag to sta drawing a structure mm Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use GO DII F5 F6 F7 F8 F9 F10 6 CO 89 & 7 LU E R T Y U 8* 9 0 D F G H J K L Z X C V B N M 36arrow_forward
- Problem 7 of 10 Draw the major product of this reaction. Ignore inorganic byproducts. S' S 1. BuLi 2. ethylene oxide (C2H4O) Select to Draw a Submitarrow_forwardFeedback (4/10) 30% Retry Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the reactant and missing intermediates involved in this reaction. Include all lone pairs and charges as appropriate. Ignore inorganic byproducts. Incorrect, 6 attempts remaining :0: Draw the Reactant H H3CO H- HIO: Ö-CH3 CH3OH2* protonation H. a H (+) H Ο CH3OH2 O: H3C protonation CH3OH deprotonation > CH3OH nucleophilic addition H. HO 0:0 Draw Intermediate a Xarrow_forwardCan I please get the blank spaces answered/answers?arrow_forward
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