![Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th](https://www.bartleby.com/isbn_cover_images/9781305081086/9781305081086_largeCoverImage.gif)
Concept explainers
(a)
Interpretation:
The name of the branched alkyl group attached to the carbon chains has to be given.
Concept Introduction:
Alkyl groups are named according to
Rule 1:
Longest continuous chain which begins at the point of attachment of the alkyl group becomes the base name for the alkyl group.
Rule 2:
Base chain that is identified is numbered in a way beginning at the point of attachment.
Rule 3:
The substituents that are present in the base chain is listed in alphabetical order using the locant as prefixes whenever necessary.
(b)
Interpretation:
The name of the branched alkyl group attached to the carbon chains has to be given.
Concept Introduction:
Alkyl groups are named according to IUPAC nomenclature. The name is obtained considering the parent alkane name and replacing “-ane” with “-yl”. In naming branched chain alkyl groups, this becomes little complicated. Hence, IUPAC system for giving name to such larger groups names them by considering as if they were themselves a separate compound. Three rules are followed while naming the larger groups.
Rule 1:
Longest continuous chain which begins at the point of attachment of the alkyl group becomes the base name for the alkyl group.
Rule 2:
Base chain that is identified is numbered in a way beginning at the point of attachment.
Rule 3:
The substituents that are present in the base chain is listed in alphabetical order using the locant as prefixes whenever necessary.
(c)
Interpretation:
The name of the branched alkyl group attached to the carbon chains has to be given.
Concept Introduction:
Alkyl groups are named according to IUPAC nomenclature. The name is obtained considering the parent alkane name and replacing “-ane” with “-yl”. In naming branched chain alkyl groups, this becomes little complicated. Hence, IUPAC system for giving name to such larger groups names them by considering as if they were themselves a separate compound. Three rules are followed while naming the larger groups.
Rule 1:
Longest continuous chain which begins at the point of attachment of the alkyl group becomes the base name for the alkyl group.
Rule 2:
Base chain that is identified is numbered in a way beginning at the point of attachment.
Rule 3:
The substituents that are present in the base chain is listed in alphabetical order using the locant as prefixes whenever necessary.
(d)
Interpretation:
The name of the branched alkyl group attached to the carbon chains has to be given.
Concept Introduction:
Alkyl groups are named according to IUPAC nomenclature. The name is obtained considering the parent alkane name and replacing “-ane” with “-yl”. In naming branched chain alkyl groups, this becomes little complicated. Hence, IUPAC system for giving name to such larger groups names them by considering as if they were themselves a separate compound. Three rules are followed while naming the larger groups.
Rule 1:
Longest continuous chain which begins at the point of attachment of the alkyl group becomes the base name for the alkyl group.
Rule 2:
Base chain that is identified is numbered in a way beginning at the point of attachment.
Rule 3:
The substituents that are present in the base chain is listed in alphabetical order using the locant as prefixes whenever necessary.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 12 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
- [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_forwardProvide 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_forward
- Steps and explanation please.arrow_forwardHow 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_forward
- Provide the unknown for the given dataarrow_forwardProvide the unknown for the given data.arrow_forwardElectron Arrangement A. Fill in the following chart relating to levels, sublevels and orbitals. Levels (n) 1 Sublevels # of Orbitals per sublevel 2 3 4 # of Electrons per sublevel Total Electrons per level Complete: B. Answer the following questions related to levels, sublevels, orbitals and electrons. 1. How many sublevels are in energy level 2? 2. How many orbitals are in a 4f sublevel? 3. How many electrons can level 3 hold? 4. How many orbitals are in level 4? 5. How many electrons can sublevel 2p hold? 11arrow_forward
- 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: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningWorld of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College Div
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305081079/9781305081079_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285853918/9781285853918_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781337399692/9781337399692_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781133109655/9781133109655_smallCoverImage.jpg)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618562763/9780618562763_smallCoverImage.gif)