(a)
Interpretation:
Condensed structural formula has to be drawn for the given
Concept Introduction:
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:
Condensed structural formula has to be drawn for the given carboxylic acid.
Concept Introduction:
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:
Condensed structural formula has to be drawn for the given carboxylic acid.
Concept Introduction:
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:
Condensed structural formula has to be drawn for the given carboxylic acid.
Concept Introduction:
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 16 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
- Please correct answer and don't used hand raitingarrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided resonance structures, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond- making steps. Incorrect, 3 attempts remaining Select to Add Arrows HO Select to Add Arrows :0 Select to Add Arrows Please help me fix this first step! Qarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the resonance hybrid contributor. Include all lone pairs and charges as appropriate. :O Please help me fix this drawing, I have attached the three incorrect drawings I've already tried. I only get one more chance! Please help! Drawing 0:0 Incorrect, 1 attempt remaining Q OCH :0: Select to Draw O :O: Select to Draw :0: Select to Drawarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- Please correct answer and don't used hand raitingarrow_forwardUse the systematic treatment of equilibrium to determine the pH and the concentrations of all species in a saturated aqueous solution of SrF2. Do not include activity coefficients. The solubility of SrF2 is governed by Ksp for the salt, hydrolysis of F- and of Sr2+, and by ion pairing between Sr2 + and F-. PK(SrF2) = 8.58, PK(HF) = 3.17, pkw = 14.00, pk for the formation of (SrOH+) = 13.18, pk for the formation of (SrF+) = 0.14 Show all your work and upload your answers here. 1 - Write the pertinent reactions. 2 - Write mass balance and charge balance equations. 3 - Write the equilibrium constant expressions. 4 - Count the equations and unknowns. 5- If the problem is solvable make suitable approximations and find the concentrations and the pH.arrow_forwardPlease correct answer and don't use hand ratingarrow_forward
- How might you prepare each of the following using a nucleophilic substitution reaction at some step? (a) (b) (c) (d) CH3 CH3C CCHCH3 CH3 CH3 0 CCH3 ☐ CH3 CH3CH2CH2CH2CN CH3CH2CH2NH2arrow_forwardNo AI response. Please reference attachment for assistance with chemistry. Will upvote if satisfied. Thanks againarrow_forwardManganese(II) Arsenate is insoluble in water at room temperature. (Note: Arsenate = AsO4³-) In the presence of aqueous ammonia, solid Manganese(II) Arsenate becomes more soluble and aqueous tetraamminemanganese (II) ion forms. When solid Manganese(II) arsenate was placed in a 2.00 M solution of ammonia, at equilibrium, 0.308 M of ammonia remains. If the Kf of tetraamminemanganese (II) ion is 250.0, Determine the Ksp of Manganese(II) arsenate Hint: You will have to figure out the Kspf of the overall chemical equation first, then solve for Ksp by using Kf and Kspfarrow_forward
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