(a)
Interpretation:
The common name for the given halogenated hydrocarbon has to be given.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as
(b)
Interpretation:
The common name for the given halogenated hydrocarbon has to be given.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
IUPAC nomenclature for halogenated alkanes/cycloalkanes:
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as alkyl halides. These are not IUPAC names. They are common names. In a common name, two parts are present. First part is the name of the hydrocarbon (alkyl group). Second part gives the halogen present in the compound. The halogen is considered as though it is present as an ion even though no ions are present.
(c)
Interpretation:
The common name for the given halogenated hydrocarbon has to be given.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
IUPAC nomenclature for halogenated alkanes/cycloalkanes:
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as alkyl halides. These are not IUPAC names. They are common names. In a common name, two parts are present. First part is the name of the hydrocarbon (alkyl group). Second part gives the halogen present in the compound. The halogen is considered as though it is present as an ion even though no ions are present.
(d)
Interpretation:
The common name for the given halogenated hydrocarbon has to be given.
Concept Introduction:
The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane. If the same is present in cycloalkane, then it is known as halogenated cycloalkane. They are product of reaction between alkane/cycloalkane with halogens.
IUPAC nomenclature for halogenated alkanes/cycloalkanes:
Similar to the alkyl groups, the halogen is also treated as substituents present on the carbon chain. They are called as fluoro-, chloro-, bromo-, and iodo-.
If the carbon chain contains both alkyl and halogen, they both are considered of equal ranks. The numbering is done in a way so that the substituents get the least number, whether it is an alkyl or a halo group.
In IUPAC names, the groups that are present on the carbon chain are written in alphabetical order.
Common names:
Halogenated alkanes are also named as alkyl halides. These are not IUPAC names. They are common names. In a common name, two parts are present. First part is the name of the hydrocarbon (alkyl group). Second part gives the halogen present in the compound. The halogen is considered as though it is present as an ion even though no ions are present.
Want to see the full answer?
Check out a sample textbook solutionChapter 12 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- IDENTIFY THE FUNCTIONAL GROUP PRESENT IN THESE COMPOUNDS. A = ? B = ? C = ?arrow_forward(a) Label all the O atoms that are part of a glycoside in rebaudioside A. Rebaudioside A, marketed under the trade name Truvia, is a sweet glycoside obtained from the stevia plant, which has been used for centuries in Paraguay to sweeten foods. (b) The alcohol or phenol formed from the hydrolysis of a glycoside is called an aglycon. What aglycon and monosaccharides are formed by the hydrolysis of rebaudioside A?arrow_forwardClassify the following lipid (choose all that apply).CHOOSE ALL THAT APPLY a. omega-6 b. trans alkene(s) c. omega-3 d. wax ester e. saturated f. monounsaturated g. fatty acid h. triglyceride i. steroid j. polyunsaturated k. cis alkene(s)arrow_forward
- Consider the intermolecular forces present in a pure sample of each of the following compounds: CH₃CH₂OH and CH₃COCH₃. Identify the intermolecular forces that these compounds have in common.arrow_forwardDefine the following terms: a. ganglioside b. sphingolipidoses c. isoprenoid d. terpene e. mixed terpenoidarrow_forwardWhich of the following is least soluble in hexane? * COOH A^ А B с E D FM COOH COOH COOH COOH 1 p COOHarrow_forward
- The ionization of p-nitrophenol is shown below (pKa = 7.0): a. Identify the weak acid and conjugate base. b. At pH 7, what are the relative concentrations of ionized and un-ionized p-nitrophenol? c. If enough concentrated hydrochloric acid is added to a solution of p-nitrophenol to lower the pH from 7 to 5, what will happen to the relative concentrations of the ionized and un-ionized forms? d. Ionized p-nitrophenol has a yellow color, while the un-ionized form is colorless. The yellow color can be measured using a spectrophotometer at 400nm. In order to determine the total amount of p-nitrophenol in a solution, would you perform the spectrophotometer reading at an acidic or basic pH? Clearly explain why? e. A solution of p-nitrophenol at pH 7.95 was found to have an A400 of 0.255 . What is the total concentration (in µM) of p-nitrophenol (ionized plus un-ionized) in the solution? The molar extinction coefficient of p-nitrophenol is 18,500 M-1cm-1 and the pKa is 7.arrow_forwardClassify the following lipid (choose all that apply for the overall structure, not the individual residues). a. wax ester b. fatty acid c. polyunsaturated d. trans alkene(s) e. steroid f. monounsaturated g. triglyceride h. cis alkene(s) i. saturatedarrow_forwardb) Determine which ionization state corresponds to aspartic acid (shown below) at pH 1, 7, and 10 by selecting the most suitable answer from the statements i-iv. The pK of the amine, carboxylic acid, and side chain of aspartic acid are 9.6, 1.88 and 3.65, respectively. ОН ÓH ÑH2 i) the amine is charged; the carboxylic acids are neutral. ii) the amine and carboxylic acids are all charged. iii) the amine is neutral, and the carboxylic acids are charged. iv) the amine and the carboxylic acids are all neutral. pH Statement (i, ii, iii, or iv) 1 7 10 %3Darrow_forward
- Consider these compounds: A. PbBr, B. MnS C. Ag,CO3 D. AIPO, Complete the following statements by entering the letter(s) corresponding to the correct compound(s). (If more than one compound fits the description, include all the relevant compounds by writing your answer as a string of characters without punctuation, e.g, ABC.) Without doing any calculations it is possible to determine that magnesium fluoride is more soluble than and magnesium fluoride is less soluble than| It is not possible to determine whether magnesium fluoride is more or less soluble than by simply comparing Kgp values.arrow_forwardIn the monosaccharide derivatives known as sugar alcohols, the carbonyl oxygen is reduced to a hydroxyl group. For example, D-glyceraldehyde can be reduced to glycerol. However, this sugar alcohol is no longer designated D or L. Why?arrow_forwardWhen Alfred Werner was developing the field of coordination chemistry, it was argued by some that the optical activity he observed in the chiral complexes he had prepared was due to the presence of carbon atoms in themolecule. To disprove this argument, Werner synthesized a chiral complex of cobalt that had no carbon atoms in it, and he was able to resolve it into its enantiomers. Design a cobalt(III) complex that would be chiral if it could be synthesized and that contains no carbon atoms.arrow_forward
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education