![Organic Chemistry, Loose-leaf Version](https://www.bartleby.com/isbn_cover_images/9781305865549/9781305865549_smallCoverImage.jpg)
Concept explainers
(a)
Interpretation:
The IUPAC name of the given compound has to be written.
Concept Introduction:
Isomers: Compounds that have same molecular formula but different structural formula.
Constitutional isomers: Compounds that have same molecular formula but different connectivity (arrangement of atoms are different).
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
(a)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (a):
In the given compound, the longest carbon chain (highlighted with bold lines) contains six carbons and while numbering the parent chain, substituents should get the least possible number.
The presence of double bond at C-2 makes parent name as 2-hexene. The substituents Bromine atom at C-2; are arranged in alphabetical order followed by the parent name.
Therefore, the systematic name of the given compounds is ‘2-bromo-2-hexene’.
(b)
Interpretation:
The IUPAC name and configuration of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
R and S nomenclature:
It is used to assign the molecule using CIP rules.
The CIP rules are as follows:
- Select the chiral carbon and assign the numbers according to the decreasing
atomic mass of atoms attached to it. - If the numbering follows clockwise direction then the atom is termed as R and if it follows anti-clockwise direction then atom is termed as S.
(b)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (b):
In the given compound, the longest carbon ring (highlighted with bold lines) contains six carbons and while numbering the parent chain, substituents should get the least possible number.
The presence of double bond at C-1 makes parent name is hex-1-ene. The substituents methyl located at C-3 and bromine atom at C-3; are arranged in alphabetical order followed by the parent name.
The chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it, follows clockwise direction then the atom is termed as R
Therefore, the systematic name of the given compounds is ‘3-bromo-3-methylcyclohex-1-ene’.
(c)
Interpretation:
The IUPAC name and configuration of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
In a cis isomer, groups are attached on the same side of the ring.
In a trans isomer, groups are attached on the opposite side of the ring.
(c)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (c):
In the given compound, the longest carbon ring (highlighted with bold lines) contains six carbons and while numbering the parent chain, substituents should get the least possible number.
The parent name is CYCLOHEXANE. The substituents bromine atoms are at C-1and C-4; are arranged in alphabetical order followed by the parent name. Here, bromine atoms are attached on the opposite side of the ring thus ‘trans’.
Therefore, the systematic name of the given compounds is ‘trans 1,4-dibromocyclohexane’.
(d)
Interpretation:
The IUPAC name of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
(d)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (d):
In the given compound, the longest carbon chain (highlighted with bold lines) contains four carbons and while numbering the parent chain, substituents should get the least possible number.
The parent name is butane. The substituents chlorine atom at C-1 and C-4; are arranged in alphabetical order followed by the parent name.
Therefore, the systematic name of the given compounds is ‘1,4-dichlorobutane’.
(e)
Interpretation:
The IUPAC name and configuration of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
R and S nomenclature:
It is used to assign the molecule using CIP rules.
The CIP rules are as follows:
- Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
- If the numbering follows clockwise direction then the atom is termed as R and if it follows anti-clockwise direction then atom is termed as S.
(e)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (e):
In the given compound, the longest carbon ring contains eight carbons and while numbering the parent chain, substituents should get the least possible number. The parent name is octane. The substituents iodine atom located at C-2; are arranged in alphabetical order followed by the parent name.
The numbering follows clockwise direction as shown above then it is termed as R. Least priority group is above the plane so the configuration is reversed.
Therefore, the systematic name of the given compounds is ‘(S)-2-iodooctane’.
(f)
Interpretation:
The IUPAC name and configuration of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
R and S nomenclature:
It is used to assign the molecule using CIP rules.
The CIP rules are as follows:
- Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
- If the numbering follows clockwise direction then the atom is termed as R and if it follows anti-clockwise direction then atom is termed as S.
(f)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (f):
In the given compound, the longest carbon ring (highlighted with bold lines) contains five carbons and while numbering the parent chain, substituents should get the least possible number.
The parent name is hexane. The substituents bromine atom located at C-2; are arranged in alphabetical order followed by the parent name.
The chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it, follows anti-clockwise direction then atom is termed as S.
Therefore, the systematic name of the given compounds is ‘(S)-2-bromopentane’.
(g)
Interpretation:
The IUPAC name and configuration of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- The complex substituent is built by a substituent on a substituent; so called complex substituent.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
R and S nomenclature:
It is used to assign the molecule using CIP rules.
The CIP rules are as follows:
- Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
- If the numbering follows clockwise direction then the atom is termed as R and if it follows anti-clockwise direction then atom is termed as S.
(g)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (g):
In the given compound, the longest carbon ring (highlighted with bold lines) contains seven carbons in a ring and while numbering the parent chain, substituents should get the least possible number.
The presence of double bond at C-1 on the ring makes parent name is cyclohept-1-ene. The substituents Fluorine atom located at C-3; are arranged in alphabetical order followed by the parent name.
The chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it, follows anti-clockwise direction then atom is termed as S. Least priority group is above the plane so the configuration is reversed. Hence, the configuration is (R).
Therefore, the systematic name of the given compounds is ‘(R)- 3-fluorocyclohept-1-ene’.
(h)
Interpretation:
The IUPAC name of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- The complex substituent is built by a substituent on a substituent; so called complex substituent.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
(h)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (h):
In the given compound, the longest carbon chain (highlighted with bold lines) contains three carbons and while numbering the parent chain, substituents should get the least possible number.
The parent name is Propane. The substituents methyl located at C-2 and bromine atom at C-1; are arranged in alphabetical order followed by the parent name.
Therefore, the systematic name of the given compounds is ‘1-bromo-2-methylpropane’.
(i)
Interpretation:
The IUPAC names and configuration of the given compound has to be written.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
(i)
![Check Mark](/static/check-mark.png)
Explanation of Solution
Compound (i):
In the given compound, the longest carbon chain (highlighted with bold lines) contains six carbons and while numbering the parent chain, substituents should get the least possible number.
The parent name is hexane. The substituents methyl located at C-5 and chlorine atom at C-2; are arranged in alphabetical order followed by the parent name.
The chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it, follows clockwise direction then the atom is termed as R.
Therefore, the systematic name of the given compounds is ‘(R)-2-chloro-5-methylhexane’.
Want to see more full solutions like this?
Chapter 8 Solutions
Organic Chemistry, Loose-leaf Version
- 3. 2. 1. On the graph below, plot the volume of rain in milliliters versus its height in centimeters for the 400 mL beaker. Draw a straight line through the points and label it "400 mL beaker." Volume (mL) 400 350 300 250 200 150 750 mL Florence Volume Versus Height of Water 400 mL beaker 100 50 0 0 2 3 4 5 Height (cm) 6 7 8 9 10 Explain why the data points for the beaker lie roughly on a straight line. What kind of relationship is this? How do you know? (see page 276 text) the design of the beaker is a uniform cylinder the volume of liquid increases evenly with its height resulting in a linear relationship. What volume would you predict for 10.0 cm of water? Explain how you arrived at your answer. Use the data table and the graph to assist you in answering the question. 4. Plot the volume of rain in milliliters versus its height in centimeters for the 250 mL Florence flask on the same graph. Draw a best-fit curve through the points and label it "250 mL Florence flask." oke camearrow_forwardShow work. Don't give Ai generated solutionarrow_forwardIn the video, we looked at the absorbance of a certain substance and how it varies depending on what wavelength of light we are looking at. Below is a similar scan of a different substance. What color BEST describes how this substance will appear? Absorbance (AU) Violet Blue Green Orange 1.2 1.0- 0.8- 0.6- 0.4- 0.2 0.0 450 500 550 600 650 700 Wavelength (nm) violet indigo blue green yellow orange red Red O Cannot tell from this information In the above graph, what causes -450 nm wavelength of light to have a higher absorbance than light with a -550 nm wavelength? Check all that are true. The distance the light travels is different The different data points are for different substances The concentration is different at different times in the experiment Epsilon (molar absortivity) is different at different wavelengthsarrow_forward
- 5. a. Data were collected for Trial 1 to determine the molar mass of a nonvolatile solid solute when dissolved in cyclo- hexane. Complete the table for the analysis (See Report Sheet). Record calculated values with the correct number of significant figures. B. Freezing Point of Cyclohexane plus Calculation Zone Unknown Solute 2. Mass of cyclohexane (g) 10.14 Part C.4 3. Mass of added solute (g) 0.255 C. Calculations 1. k; for cyclohexane (°C⚫ kg/mol) 20.0 2. Freezing point change, AT, (°C) 3.04 Part C.6 3. Mass of cyclohexane in solution (kg) 4. Moles of solute, total (mol) Show calculation. 5. Mass of solute in solution, total (g) 6. Molar mass of solute (g/mol) Show calculation.arrow_forwardDraw and name the R groups of all 20 amino acids.arrow_forward3. Two solutions are prepared using the same solute: Solution A: 0.14 g of the solute dissolves in 15.4 g of t-butanol Solution B: 0.17 g of the solute dissolves in 12.7 g of cyclohexane Which solution has the greatest freezing point change? Show calculations and explain.arrow_forward
- 2. Give the ground state electron configuration (e.g., 02s² σ*2s² П 2p²) for these molecules and deduce its bond order. Ground State Configuration Bond Order H2+ 02- N2arrow_forward1. This experiment is more about understanding the colligative properties of a solution rather than the determination of the molar mass of a solid. a. Define colligative properties. b. Which of the following solutes has the greatest effect on the colligative properties for a given mass of pure water? Explain. (i) 0.01 mol of CaCl2 (ii) 0.01 mol of KNO3 (iii) 0.01 mol of CO(NH2)2 (an electrolyte) (an electrolyte) (a nonelectrolyte)arrow_forward5. b. For Trials 2 and 3, the molar mass of the solute was 151 g/mol and 143 g/mol respectively. a. What is the average molar mass of the solute ? b. What are the standard deviation and the relative standard deviation (%RSD) for the molar mass of the solute ?arrow_forward
- Show work. Don't give Ai generated solutionarrow_forward2. Explain why ice cubes formed from water of a glacier freeze at a higher temperature than ice cubes formed from water of an under- ground aquifer. Photodynamic/iStockphotoarrow_forwardShow reaction mechanism. don't give Ai generated solutionarrow_forward
- Organic 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/9781305580350/9781305580350_smallCoverImage.gif)