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Anethole, the major constituent of anise oil, is used in licorice-flavored sweets and flavored brandy. Answer the following questions using the ball-and-stick model of anethole.
- What is the molecular formula of anethole?
![Check Mark](/static/check-mark.png)
(a)
Interpretation:
The molecular formula of anethole should be determined.
Concept Introduction:
The numbers and kinds of atoms present in a molecule of a compound are given by a formula said to be a molecular formula. This formula of a molecule gives the definite number of atoms of each element present in the compound.
Answer to Problem 13.29P
The molecular formula of anethole is C10H12O.
Explanation of Solution
The given ball-and-stick model of anethole is:
In ball-and-stick model, the black ball represents carbon, C atom, white ball represents hydrogen, H atom, and red ball represents oxygen, O atom.
The number of each atom in the ball-and-stick model is:
Carbon atoms = 10
Hydrogen atoms = 12
Oxygen atom = 1
Thus, the molecular of anethole is C10H12O.
![Check Mark](/static/check-mark.png)
(b)
Interpretation:
The functional group(s) in anethole should be determined.
Concept Introduction:
A group of atoms or an atom which is responsible for the characteristic reactions of a particular compound is said to be the functional group. Every functional group shows distinctive chemical properties irrespective to the moiety to which it is attached.
Answer to Problem 13.29P
The functional group(s) in anethole is ether.
Explanation of Solution
The given ball-and-stick model of anethole is:
When the oxygen atom is connected to two alkyl or aryl groups with general formula R-O-R' such class of compounds is known as ether.
Since, in anethole compound the oxygen atom is bonded to an aryl and an alkyl group so, the functional group(s) in anethole is ether.
![Check Mark](/static/check-mark.png)
(c)
Interpretation:
The carbon-carbon double bond in anethole should be labeled as cis or trans.
Concept Introduction:
The molecule with same molecular formula and connectivity but differ in spatial arrangements of atoms in the molecule are said to be geometric isomers of each other.
Answer to Problem 13.29P
The carbon-carbon double bond in anethole is labeled as trans.
Explanation of Solution
The given ball-and-stick model of anethole is:
Geometric isomerism, or cis-trans, isomerism is most common in alkenes. The two forms exist due to no free rotation about carbon-carbon double bond. It exists only when the double bonded carbon atoms are joined to two different groups or atoms.
In cis- isomer, the two identical groups or atoms are close to each other whereas in trans- isomer two identical groups or atoms are farther apart.
Since, in the given molecule the groups attached to carbon-carbon double bonded are farther apart from each other so, the carbon-carbon double bond in anethole is trans.
![Check Mark](/static/check-mark.png)
(d)
Interpretation:
The structure of anethole should be drawn and each carbon should be labeled as trigonal planar or tetrahedral.
Concept Introduction:
In structural formula, the bonding and type of bonds which holds the atoms in molecule together are shown.
Answer to Problem 13.29P
The structure of anethole is:
Labelling of each carbon is:
Explanation of Solution
The given ball-and-stick model of anethole is:
In ball-and-stick model, the black ball represents carbon, C atom, white ball represents hydrogen, H atom, and red ball represents oxygen, O atom.
So, the structure of anethole is:
In the structure of anethole, there are 10 C atoms, 2 of which them are in CH3- groups which has four electron groups around the central carbon atom, so the electron group arrangement is tetrahedral, sp3hybridized. The 8 carbon atoms have three electron groups around the central carbon atom, so the electron group arrangement is trigonal planar, sp2hybridized.
Thus, the electron group arrangement of all the 10 carbon atoms in anethole is:
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Chapter 13 Solutions
EBK GENERAL, ORGANIC, & BIOLOGICAL CHEM
- I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."arrow_forwardShow work with explanation. Don't give Ai generated solutionarrow_forwardShow work. don't give Ai generated solutionarrow_forward
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