(a)
Interpretation:
The given line-angle structural formula has to be converted to condensed structural formula.
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:
The given line-angle structural formula has to be converted to condensed structural formula.
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:
The given line-angle structural formula has to be converted to condensed structural formula.
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:
The given line-angle structural formula has to be converted to condensed structural formula.
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.
Trending nowThis is a popular solution!
Chapter 12 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- ii) Molecular ion peak :the peak corresponding to the intact molecule (with a positive charge) What would the base peak and Molecular ion peaks when isobutane is subjected to Mass spectrometry? Draw the structures and write the molecular weights of the fragments. Circle most stable cation a) tert-butyl cation b) Isopropyl cation c) Ethyl cation. d) Methyl cation 6. What does a loss of 15 represent in Mass spectrum? a fragment of the molecule with a mass of 15 atomic mass units has been lost during the ionization Process 7. Write the isotopes and their % abundance of isotopes of i) Clarrow_forwardChoose a number and match the atomic number to your element on the periodic table. For your element, write each of these features on a side of your figure. 1. Element Name and symbol 2. Family and group 3. What is it used for? 4. Sketch the Valence electron orbital 5. What ions formed. What is it's block on the periodic table. 6. Common compounds 7. Atomic number 8. Mass number 9. Number of neutrons- (show calculations) 10. Sketch the spectral display of the element 11.Properties 12. Electron configuration 13. Submit a video of a 3-meter toss in slow-moarrow_forward[In this question, there are multiple answers to type in a "fill-in-the-blank" fashion - in each case, type in a whole number.] Consider using Slater's Rules to calculate the shielding factor (S) for the last electron in silicon (Si). There will be electrons with a 0.35 S-multiplier, electrons with a 0.85 S-multiplier, and electrons with a 1.00 S-multiplier.arrow_forward
- Provide the unknown for the given data.arrow_forwardDraw the Lewis structures of two methanol (CH3OH) molecules and depict hydrogenbonding between them with dashed lines. Show all lone pairs. Provide a thorough analysis to apply concept idea into other problems.arrow_forwardSteps and explanation please.arrow_forward
- How could you distinguish between each pair of compounds below using IR? For each pair citeone bond and it’s frequency that you could use to distinguish between them. Please provide thorough analysis to apply into further problems.arrow_forwardSteps and explanation please.arrow_forwardSteps and explanation on how to solve.arrow_forward
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co