a. Identify the functional groups in the ball-and-stick model of elemicin, a compound partly responsible f or the flavor and fragrance of nutmeg.
b. Draw a skeletal structure of a constitutional isomer of elemicin that should have a higher boiling point and melting point.
c. Label all electrophilic carbon atoms.
![Check Mark](/static/check-mark.png)
(a)
Interpretation: The functional groups in the ball-and-stick model of elemicin are to be identified.
Concept introduction: An atom or a group of atoms which are responsible for characteristic physical and chemical properties of the compound are collectively known as functional groups. The functional groups are the most reactive part present in the molecule.
Answer to Problem 31P
The functional groups present in the ball-and-stick model of elemicin are ether and alkene group.
Explanation of Solution
The given molecule is,
Figure 1
The red coloured balls have two bonds. So, these are the oxygen atoms. Black coloured atoms have four bonds. So, these are the carbon atoms. The grey coloured balls have one bond. So, these are the hydrogen atoms. The molecular structure of elemicin is,
Figure 2
The functional groups present in the ball-and-stick model of elemicin are ether and alkene group.
The functional groups present in the ball-and-stick model of elemicin are ether and alkene group.
![Check Mark](/static/check-mark.png)
(b)
Interpretation: The skeletal structure of a constitutional isomer of elemicin that should have a higher boiling point and melting point is to be drawn.
Concept introduction: The isomers which have same molecular formula but different connectivity of atoms are constitutional isomers.
The temperature at which the vapour pressure of a substance becomes equal to the pressure surrounding the liquid is boiling point. The boiling point depends on the intermolecular forces. Stronger the intermolecular force, higher is the boiling point.
The temperature at which the solid converts to its liquid phase is melting point. Stronger the intermolecular force, higher is the boiling point.
Answer to Problem 31P
The skeletal structure of a constitutional isomer of elemicin that should have a higher boiling point and melting point is shown below.
Explanation of Solution
The skeletal structure of a constitutional isomer of elemicin that should have a higher boiling point and melting point is,
Figure 3
This structure contains alcohol groups. This structure exhibits intermolecular hydrogen bonding due to the presence of hydrogen atoms bonded to oxygen atom. Hydrogen bonding is strongest intermolecular forces.
The skeletal structure of a constitutional isomer of elemicin that should have a higher boiling point and melting point is shown in Figure 3.
![Check Mark](/static/check-mark.png)
(c)
Interpretation: All electrophilic carbon atoms are to be labeled.
Concept introduction: An electron deficient due to hetero atoms or pi bonds or both is electrophilic site and an electron rich site due to hetero atoms or pi bonds or both is nucleophilic site.
Answer to Problem 31P
The carbon atoms attached to the oxygen atom in ether group are electrophilic in nature.
Explanation of Solution
An oxygen atom is more electronegative than carbon atom which makes the carbon atom attached to oxygen atom electron deficient and electrophilic site as shown below.
Figure 4
The carbon atoms attached to the oxygen atom in ether group are electrophilic in nature.
Want to see more full solutions like this?
Chapter 3 Solutions
Connect Online Access 1-Semester for Organic Chemistry
- 6. How many peaks would be observed for each of the circled protons in the compounds below? 8 pts CH3 CH3 ΤΙ A. H3C-C-C-CH3 I (₁₁ +1)= 7 H CI B. H3C-C-CI H (3+1)=4 H LIH)=2 C. (CH3CH2-C-OH H D. CH3arrow_forwardNonearrow_forwardQ1: Draw the most stable and the least stable Newman projections about the C2-C3 bond for each of the following isomers (A-C). Are the barriers to rotation identical for enantiomers A and B? How about the diastereomers (A versus C or B versus C)? H Br H Br (S) CH3 (R) CH3 H3C (S) H3C H Br Br H A C enantiomers H Br H Br (R) CH3 H3C (R) (S) CH3 H3C H Br Br H B D identicalarrow_forward
- 2. Histamine (below structure) is a signal molecule involved in immune response and is a neurotransmitter. Histamine features imidazole ring which is an aromatic heterocycle. Please answer the following questions regarding Histamine. b a HN =N C NH2 a. Determine hybridization of each N atom (s, p, sp, sp², sp³, etc.) in histamine N-a hybridization: N-b hybridization: N-c hybridization: b. Determine what atomic orbitals (s, p, sp, sp², sp³, etc.) of the lone pair of each N atom resided in N-a hybridization: N-b hybridization: N-c hybridization:arrow_forwardNonearrow_forward29. Use frontier orbital analysis (HOMO-LUMO interactions) to decide whether the following dimerization is 1) thermally allowed or forbidden and 2) photochemically allowed or forbidden. +arrow_forward
- 30.0 mL of 0.10 mol/L iron sulfate and 20.0 mL of 0.05 mol/L of silver nitrate solutions are mixed together. Justify if any precipitate would formarrow_forwardDoes the carbonyl group first react with the ethylene glycol, in an intermolecular reaction, or with the end alcohol, in an intramolecular reaction, to form a hemiacetal? Why does it react with the alcohol it does first rather than the other one? Please do not use an AI answer.arrow_forwardThe number of noncyclic isomers that have the composition C4H8Owith the O as part of an OH group, counting a pair of stereoisomers as1, is A. 8; B. 6; C. 9; D. 5; E. None of the other answers is correct.arrow_forward
- Nonearrow_forwardThe number of carbon skeletons that have 8 carbons, one of which istertiary is A. 7; B. More than 7; C. 6; D. 5; E. 4arrow_forwardThe azide ion is N3^-. In addition to the ionic charge, it’s three mostimportant contributing structures also have formal charges. The totalnumber of π bonds in these three contributing structures isA. 6; B. 12; C. 3; D. 9; E. None of the other answers is correct.arrow_forward
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781133109655/9781133109655_smallCoverImage.jpg)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)