
Concept explainers
(a)
Interpretation:
The complete IUPAC name for the given molecule is to be written.
Concept introduction:
When assigning priorities to substituents, the atom having the greater
(b)
Interpretation:
The complete IUPAC name for the given molecule is to be written.
Concept introduction:
When assigning priorities to substituents, the atom having the greater atomic number has a higher priority. In the case of comparison between isotopes, the one having the greater atomic mass gets the higher priority. If the substituents are attached by the same atom, then the set of atoms one bond away from the point of attachment are compared. In each set, the highest priority atoms are compared. If the sets of atoms one bond away from the point of attachment are identical, then the sets of atoms one additional bond away from the point of attachment are compared. If the higher priority groups attached to the double bonded carbon atoms are on the same side of the double bond, the alkene is assigned Z configuration. If the higher priority groups attached to the double bonded carbon atoms are on the opposite side of the double bond, the alkene is assigned E configuration. When more than one double bond is present, each is assigned E or Z configuration, and the location of each double bond appears immediately before the E or Z designation.
(c)
Interpretation:
The complete IUPAC name for the given molecule is to be written.
Concept introduction:
When assigning priorities to substituents, the atom having the greater atomic number has a higher priority. In the case of comparison between isotopes, the one having the greater atomic mass gets the higher priority. If the substituents are attached by the same atom, then the set of atoms one bond away from the point of attachment is compared. In each set, the highest priority atoms are compared. If the sets of atoms one bond away from the point of attachment are identical, then the sets of atoms one additional bond away from the point of attachment are compared. If the higher priority groups attached to the double bonded carbon atoms are on the same side of the double bond, the alkene is assigned Z configuration. If the higher priority groups attached to the double bonded carbon atoms are on the opposite side of the double bond, the alkene is assigned E configuration. When more than one double bond is present, each is assigned E or Z configuration, and the location of each double bond appears immediately before the E or Z designation.
(d)
Interpretation:
The complete IUPAC name for the given molecule is to be written.
Concept introduction:
When assigning priorities to substituents, the atom having the greater atomic number has a higher priority. In the case of comparison between isotopes, the one having the greater atomic mass gets the higher priority. If the substituents are attached by the same atom, then the set of atoms one bond away from the point of attachment is compared. In each set, the highest priority atoms are compared. If the sets of atoms one bond away from the point of attachment are identical, then the sets of atoms one additional bond away from the point of attachment are compared. If the higher priority groups attached to the double bonded carbon atoms are on the same side of the double bond, the alkene is assigned Z configuration. If the higher priority groups attached to the double bonded carbon atoms are on the opposite side of the double bond, the alkene is assigned E configuration. When more than one double bond is present, each is assigned E or Z configuration, and the location of each double bond appears immediately before the E or Z designation.

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Chapter C Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
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- For CARS, which statement is not true regarding its advantages? a) Contrast signal based on vibrational characteristics, no need for fluorescent tagging. b) Stronger signals than spontaneous Raman. c) Suffers from fluorescence interference, because CARS signal is at high frequency. d) Faster, more efficient imaging for real-time analysis. e) Higher resolution than spontaneous Raman microscopy.arrow_forwardDraw the major product of the Claisen condensation reaction between two molecules of this ester. Ignore inorganic byproducts. Incorrect, 5 attempts remaining 1. NaOCH3/CH3OH 2. Acidic workup Select to Draw O Incorrect, 5 attempts remaining The total number of carbons in the parent chain is incorrect. Review the reaction conditions including starting materials and/or intermediate structures and recount the number of carbon atoms in the parent chain of your structure. OKarrow_forwardUsing a cell of known pathlength b = 1.25115 x 10-3 cm, a water absorption spectrum was measured. The band at 1645 cm-1, assigned to the O-H bending, showed an absorbance, A, of 1.40. a) Assuming that water density is 1.00 g/mL, calculate the water molar concentration c (hint: M= mole/L) b) Calculate the molar absorptivity, a, of the 1645 cm-1 band c) The transmitted light, I, can be written as I= Ioexp(-xb), where x is the absorption coefficient (sometimes designated as alpha), Io is the input light, and b is the cell pathlength. Prove that x= (ln10)*x*c d) Calculate x for the 1645 cm-1 bandarrow_forward
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