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Concept explainers
Interpretation:
The IUPAC name of the given compound is to be written.
Concept introduction:
The root name is determined by the number of carbon atoms in the longest straight chain as an
(b)
Interpretation:
The IUPAC name of the given compound is to be written.
Concept introduction:
The root name is determined by the number of carbon atoms in the longest straight chain as an alkane. In the case of a ring compound, the root name is cycloalkane. When the compound contains both a ring and a straight chain, the root depends on which of the two contains more carbon atoms. If the ring is smaller, then it is treated as a substituent, and named cycloalkyl. Any substituents are then numbered and named at the start of the complete name. The numbering of the substituents is done so as to get the smallest possible numbers. If more than one type of substituents is present, then they are listed alphabetically.
When an alkyl chain is attached to the root at a carbon other than the end carbon (#1), the longest chain of the substituent is determined from the point of attachment. The remaining part of the chain is treated as a substituent on this chain.
(c)
Interpretation:
The IUPAC name of the given compound is to be written.
Concept introduction:
The root name is determined by the number of carbon atoms in the longest straight chain as an alkane. In the case of a ring compound, the root name is cycloalkane. When the compound contains both a ring and a straight chain, the root depends on which of the two contains more carbon atoms. If the ring is smaller, then it is treated as a substituent, and named cycloalkyl. Any substituents are then numbered and named at the start of the complete name. The numbering of the substituents is done so as to get the smallest possible numbers. If more than one type of substituents is present, then they are listed alphabetically.
When an alkyl chain is attached to the root at a carbon other than the end carbon (#1), the longest chain of the substituent is determined from the point of attachment. The remaining part of the chain is treated as a substituent on this chain.
(d)
Interpretation:
The IUPAC name of the given compound is to be written.
Concept introduction:
The root name is determined by the number of carbon atoms in the longest straight chain as an alkane. In the case of a ring compound, the root name is cycloalkane. When the compound contains both a ring and a straight chain, the root depends on which of the two contains more carbon atoms. If the ring is smaller, then it is treated as a substituent, and named cycloalkyl. Any substituents are then numbered and named at the start of the complete name. The numbering of the substituents is done so as to get the smallest possible numbers. If more than one type of substituents is present, then they are listed alphabetically.
When an alkyl chain is attached to the root at a carbon other than the end carbon (#1), the longest chain of the substituent is determined from the point of attachment. The remaining part of the chain is treated as a substituent on this chain.
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Chapter A Solutions
Get Ready for Organic Chemistry
- Nonearrow_forwardDraw the structure of the product of the reaction given the IR and MS data. Spectral analysis of the product reveals: MS: M 150, M-15, M-43 CH.COCI AICI, IR: 3150-3000 cm, 2950-2850 cm and 1700 cmarrow_forwardPart II. Identify whether the two protons in blue are homotopic, enantiopic, diasteriotopic, or heterotopic. a) HO b) Bri H HH c) d) H H H Br 0arrow_forward
- Nonearrow_forwardChoose the option that is decreasing from biggest to smallest. Group of answer choices: 100 m, 10000 mm, 100 cm, 100000 um, 10000000 nm 10000000 nm, 100000 um, 100 cm, 10000 mm, 100 m 10000000 nm, 100000 um, 10000 mm, 100 cm, 100 m 100 m, 100 cm, 10000 mm, 100000 um, 10000000 nmarrow_forwardQ1. (a) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH3. Use curved arrows to show the electron movement. (b) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH4*. Use curved arrows to show the electron movement.arrow_forward
- Part II. count the expected number of signals in the 1H-NMR spectrum of these compounds HO 0 одев * Cl -cl "D"arrow_forwardPart I. Create a splitting tree diagram to predict the multiplet pattern of proton Hb in the compound below: 3 (Assume that "Jab >>> ³JbC) Ha Hb He он Ha NH2 Ha HCarrow_forwardNonearrow_forward
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