(a)
Interpretation:
Bond-line structure of the molecules should be drawn for the given IUPAC names.
Concept introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the parent chain.
Suffix denotes the presence of
Root word represents the longest continuous carbon skeleton of the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with Cyclo.
The structure of a molecule can be drawn by analyzing the presence of prefix, suffix and root word in the given IUPAC name.
In bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, they are drawn as line segments. For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a labelled line segment.
(a)
Answer to Problem 32PP
Answer
(a)
Explanation of Solution
Explanation
To analyze the presence of prefix suffix and root name in the given IUPAC name and draw the bond- line structure of the molecule (a).
The given IUPAC name is 1,4-Cyclohexadiene.
The given IUPAC Name is 1, 4-Cyclohexadiene. In the IUPAC name 1,4 represents the position of substituents or functional group in the molecule. But no substituents presented in the name, so the 1,4 positions are locating the function groups.
The root word cyclohex indicates the molecule contains 6 carbons and the cyclo indicates the molecule is cyclic. The suffix ‘diene’ denotes the molecule is alkene and the number ‘1,4’just before the root name represent the positions of double bonds.
Therefore the bond- line structure of the molecule (a) is shown below.
(b)
Interpretation:
Bond-line structure of the molecules should be drawn for the given IUPAC names.
Concept introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the parent chain.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. The position of this fictional group is represented just before the root name.
Root word represents the longest continuous carbon skeleton of the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with Cyclo.
The structure of a molecule can be drawn by analyzing the presence of prefix, suffix and root word in the given IUPAC name.
In bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, they are drawn as line segments. For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a labelled line segment.
(b)
Answer to Problem 32PP
Answer
Explanation of Solution
Explanation
To analyze the presence of prefix suffix and root name in the given IUPAC name and draw the bond- line structure of the molecule (b).
The given IUPAC name is 1, 3-Cyclohexadiene.
The given IUPAC Name is 1, 3-Cyclohexadiene. In the IUPAC name 1,3 represents the position of substituents or functional group in the molecule. But no substituents presented in the name, so the 1, 3 positions are locating the function groups.
The root word cyclohex, indicates the molecule contains 6 carbons and the cyclo indicates the molecule is cyclic, the suffix ‘diene’ denotes the molecule is alkene and the number ‘1,3’just before the root name represent the positions of double bonds.
Therefore the bond- line structure of the molecule (b) is shown below.
(c)
Interpretation:
Bond-line structure of the molecules should be drawn for the given IUPAC names.
Concept introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the parent chain.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. The position of this fictional group is represented just before the root name.
Root word represents the longest continuous carbon skeleton of the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with Cyclo.
The structure of a molecule can be drawn by analyzing the presence of prefix, suffix and root word in the given IUPAC name.
In bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, they are drawn as line segments. For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a labelled line segment.
(c)
Answer to Problem 32PP
Answer
Explanation of Solution
Explanation
To analyze the presence of prefix suffix and root name in the given IUPAC name and draw the bond- line structure of the molecule (c).
The given IUPAC name is (z)-1, 3-Pentadiene.
The given IUPAC Name is (z)-1, 3-Pentadiene.
In the IUPAC name 1, 3 represent the position of substituents or functional groups in the molecule. In the IUPAC name 1, 3 represent the position of substituents or functional group in the molecule. But no substituents presented in the name, so the 1,3 positions are locating the function groups.
The word pent indicates the molecule contains 5 carbons. The suffix ‘diene’ denotes the molecule is alkene and the number ‘1, 3’ just before the root name represents the positions of double bonds. The prefix ‘z’ is a stereo-descriptor for the double bond, which indicates the non-similar groups are attached to double bond on same sides.
Hence the bond- line structure for the given IUPAC name is
(d)
Interpretation:
Bond-line structure of the molecules should be drawn for the given IUPAC names.
Concept introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the parent chain.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. The position of this fictional group is represented just before the root name.
Root word represents the longest continuous carbon skeleton of the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with Cyclo.
The structure of a molecule can be drawn by analyzing the presence of prefix, suffix and root word in the given IUPAC name.
In bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, they are drawn as line segments. For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a labelled line segment.
(d)
Answer to Problem 32PP
Answer
Explanation of Solution
Explanation
To analyze the presence of prefix suffix and root name in the given IUPAC name and draw the bond- line structure of the molecule (d).
The given IUPAC name is (2Z, 4E)-Hepta-2,4-diene.
The given IUPAC Name is (2Z, 4E)-Hepta-2,4-diene.
The word Hepta indicates the molecule contains 7 carbons. The suffix ‘diene’ denotes the molecule is alkene and the number ‘2, 4’ just before the root name represents the positions of double bonds. The prefix ‘2Z,4E’ is the stereo-descriptor for the double bonds, which indicates the non-similar groups attached to 2-positioned double bond are on same sides and the non-similar groups attached to 4-positioned double bond are on opposite sides.
Hence the bond- line structure for the given IUPAC name is
(e)
Interpretation:
Bond-line structure of the molecules should be drawn for the given IUPAC names.
Concept introduction:
Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule and its position in the parent chain.
Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc. The position of this fictional group is represented just before the root name.
Root word represents the longest continuous carbon skeleton of the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with Cyclo.
The structure of a molecule can be drawn by analyzing the presence of prefix, suffix and root word in the given IUPAC name.
In bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, they are drawn as line segments. For acyclic carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a labelled line segment.
(e)
Answer to Problem 32PP
Answer
Explanation of Solution
Explanation
To analyze the presence of prefix suffix and root name in the given IUPAC name and draw the bond- line structure of the molecule (e).
The given IUPAC name is 2, 3–Dimethyl-1, 3-butadiene.
The given IUPAC Name is 2, 3–Dimethyl-1, 3-butadiene.
In the IUPAC name 2, 3 represent the position of substituents in the molecule. Dimethyl is the prefix that indicates the presence of two methyl groups in the molecule.
The word but indicates the molecule contains 4 carbons. The suffix diene denotes the molecule is alkene and the number ‘2, 3’ just before the root name represents the positions of double bonds.
Hence the bond- line structure for the given IUPAC name is
Want to see more full solutions like this?
Chapter 17 Solutions
Organic Chemistry, Binder Ready Version
- 4. Propose a synthesis of the target molecules from the respective starting materials. a) b) LUCH C Br OHarrow_forwardThe following mechanism for the gas phase reaction of H2 and ICI that is consistent with the observed rate law is: step 1 step 2 slow: H2(g) +ICI(g) → HCl(g) + HI(g) fast: ICI(g) + HI(g) → HCl(g) + |2(g) (1) What is the equation for the overall reaction? Use the smallest integer coefficients possible. If a box is not needed, leave it blank. + → + (2) Which species acts as a catalyst? Enter formula. If none, leave box blank: (3) Which species acts as a reaction intermediate? Enter formula. If none, leave box blank: (4) Complete the rate law for the overall reaction that is consistent with this mechanism. (Use the form k[A][B]"..., where '1' is understood (so don't write it) for m, n etc.) Rate =arrow_forwardPlease correct answer and don't use hand rating and don't use Ai solutionarrow_forward
- 1. For each of the following statements, indicate whether they are true of false. ⚫ the terms primary, secondary and tertiary have different meanings when applied to amines than they do when applied to alcohols. • a tertiary amine is one that is bonded to a tertiary carbon atom (one with three C atoms bonded to it). • simple five-membered heteroaromatic compounds (e.g. pyrrole) are typically more electron rich than benzene. ⚫ simple six-membered heteroaromatic compounds (e.g. pyridine) are typically more electron rich than benzene. • pyrrole is very weakly basic because protonation anywhere on the ring disrupts the aromaticity. • thiophene is more reactive than benzene toward electrophilic aromatic substitution. • pyridine is more reactive than nitrobenzene toward electrophilic aromatic substitution. • the lone pair on the nitrogen atom of pyridine is part of the pi system.arrow_forwardThe following reactions are NOT ordered in the way in which they occur. Reaction 1 PhO-OPh Reaction 2 Ph-O -CH₂ heat 2 *OPh Pho -CH2 Reaction 3 Ph-O ⚫OPh + -CH₂ Reaction 4 Pho Pho + H₂C OPh + CHOPh H₂C -CH₂ Reactions 1 and 3 Reaction 2 O Reaction 3 ○ Reactions 3 and 4 ○ Reactions 1 and 2 Reaction 4 ○ Reaction 1arrow_forwardSelect all possible products from the following reaction: NaOH H₂O a) b) ОН HO O HO HO e) ОН f) O HO g) h) + OHarrow_forward
- 3. Draw diagrams to represent the conjugation in these molecules. Draw two types of diagram: a. Show curly arrows linking at least two different ways of representing the molecule b. Indicate with dotted lines and partial charges (where necessary) the partial double bond (and charge) distribution H₂N* H₂N -NH2arrow_forwardQuestion 2 of 25 point Question Attempt 3 of Ulimited Draw the structure for 3-chloro-4-ethylheptane. Part 2 of 3 Click and drag to start drawing a structure. Draw the structure for 1-chloro-4-ethyl-3-lodooctane. Click and drag to start drawing a structure. X G X B c Part 3 of 30 Draw the structure for (R)-2-chlorobutane. Include the stereochemistry at all stereogenic centers. Check Click and drag to start drawing a structure. G X A 。 MacBook Pro G P Save For Later Submit Assignment Privacyarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- In a silicon and aluminum alloy, with 12.6% silicon, what are the approximate percentages of the phases present in the constituent that is formed at the end of solidification? Temperature (°C) 1500 1000 L B+L 1415- α+L 577' 500 1.65 12.6 99.83 α+B B 0 Al 20 40 60 Weight percent silicon 80 Siarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY