![ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<](https://www.bartleby.com/isbn_cover_images/9781259972348/9781259972348_largeCoverImage.gif)
Write structural formulas for all the constitutionally isomeric alcohols of molecular
formula
![Check Mark](/static/check-mark.png)
Interpretation:
The structural formulas for the constitutionally isomeric alcohols of molecular formula
Concept Introduction:
Isomers that have the same molecular formula but differ in the way in which different atoms are connected are known as constitutional isomers.
The number of atoms of each element present in the compound, is known as the molecular formula.
When the functional group
Answer to Problem 22P
Solution:
There are 8 constitutionally isomeric alcohols of molecular formula
Substitutive name:
Functional class name: pentyl alcohol
It is a primary alcohol.
Substitutive name:
Functional class name:
It is a secondary alcohol.
Substitutive name:
Functional class name:
It is a secondary alcohol.
Substitutive name:
Functional class name:
It is a primary alcohol.
Substitutive name:
Functional class name:
It is a primary alcohol.
Substitutive name:
Functional class name:
It is a tertiary alcohol.
Substitutive name:
Functional class name:
It is a secondary alcohol.
Substitutive name:
Functional class name:
It is a primary alcohol.
Explanation of Solution
In all, there are
They have the same molecular formula but different connectivity of atoms.
The structural formulas of these alcohols can be written as follows.
The substitutive name of this alcohol is
The functional class name of this alcohol is pentyl alcohol.
The hydroxyl group is attached to a primary carbon atom. Hence, it is a primary alcohol.
The substitutive name of this alcohol is
The functional class name of this alcohol is
The hydroxyl group is attached to a secondary carbon atom. Hence, it is a secondary alcohol.
The substitutive name of this alcohol is
The functional class name of this alcohol is
The hydroxyl group is attached to a secondary carbon atom. Hence, it is a secondary alcohol.
The substitutive name of this alcohol is
The functional class name of this alcohol is
The hydroxyl group is attached to a primary carbon atom. Hence, it is a primary alcohol.
The substitutive name of this alcohol is
The functional class name of this alcohol is
The hydroxyl group is attached to a primary carbon atom. Hence, it is a primary alcohol.
The substitutive name of this alcohol is 2-methyl-2-butanol.
The functional class name of this alcohol is 1,1-dimethylpropanol.
The hydroxyl group is attached to a tertiary carbon atom. Hence, it is a tertiary alcohol.
The substitutive name of this alcohol is
The functional class name of this alcohol is
The hydroxyl group is attached to a secondary carbon atom. Hence, it is a secondary alcohol.
The substitutive name of this alcohol is
The functional class name of this alcohol is
The hydroxyl group is attached to a primary carbon atom. Hence, it is a primary alcohol.
The structural formulas for the constitutionally isomeric alcohols of molecular formula
Want to see more full solutions like this?
Chapter 5 Solutions
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
- The emission data in cps displayed in Table 1 is reported to two decimal places by the chemist. However, the instrument output is shown in Table 2. Table 2. Iron emission from ICP-AES Sample Blank Standard Emission, cps 579.503252562 9308340.13122 Unknown Sample 343.232365741 Did the chemist make the correct choice in how they choose to display the data up in Table 1? Choose the best explanation from the choices below. No. Since the instrument calculates 12 digits for all values, they should all be kept and not truncated. Doing so would eliminate significant information. No. Since the instrument calculates 5 decimal places for the standard, all of the values should be limited to the same number. The other decimal places are not significant for the blank and unknown sample. Yes. The way Saman made the standards was limited by the 250-mL volumetric flask. This glassware can report values to 2 decimal places, and this establishes our number of significant figures. Yes. Instrumental data…arrow_forwardSteps and explanation pleasearrow_forwardSteps and explanation to undertand concepts.arrow_forward
- Nonearrow_forward7. Draw a curved arrow mechanism for the following reaction. HO cat. HCI OH in dioxane with 4A molecular sievesarrow_forwardTry: Convert the given 3D perspective structure to Newman projection about C2 - C3 bond (C2 carbon in the front). Also, show Newman projection of other possible staggered conformers and circle the most stable conformation. Use the template shown. F H3C Br Harrow_forward
- Nonearrow_forward16. Consider the probability distribution p(x) = ax", 0 ≤ x ≤ 1 for a positive integer n. A. Derive an expression for the constant a, to normalize p(x). B. Compute the average (x) as a function of n. C. Compute σ2 = (x²) - (x)², the variance of x, as a function of n.arrow_forward451. Use the diffusion model from lecture that showed the likelihood of mixing occurring in a lattice model with eight lattice sites: Case Left Right A B C Permeable Barrier → and show that with 2V lattice sites on each side of the permeable barrier and a total of 2V white particles and 2V black particles, that perfect de-mixing (all one color on each side of the barrier) becomes increasingly unlikely as V increases.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079243/9781305079243_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781133611097/9781133611097_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781337399074/9781337399074_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781133949640/9781133949640_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305580350/9781305580350_smallCoverImage.gif)