Concept explainers
(a)
Interpretation:
E or Z configuration is to be assigned to each double bond wherever appropriate in the given molecule.
Concept introduction:
When assigning priorities to substituents, the atom having the greater
(b)
Interpretation:
E or Z configuration is to be assigned to each double bond wherever appropriate in the given molecule.
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.
(c)
Interpretation:
E or Z configuration is to be assigned to each double bond wherever appropriate in the given molecule.
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
ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
- How many chiral centers are there in the following molecule? HO 0 1 ○ 2 ♡ 4 'N'arrow_forwardThe following chemical structure represents a molecule of what molecular formula?arrow_forwardWhich region(s) of the following phospholipid is/are hydrophobic? RO I hydro-water phobic-dislikes = Hydrophobic dislikes water ○ I only Il only I and III only II and IV only O II, III, and IV only III || IVarrow_forward
- Given the following data, determine the order of the reaction with respect to H2. H2(g) + 21Cl(g) → I2(g) + 2HCl(g) Experiment [H2] (torr) [ICI] (torr) Rate (M/s) 1 250 325 0.266 2 250 81 0.0665 3 50 325 0.266arrow_forwardWhich one of the following molecules is chiral? H- NH₂ H3C དང་།་ OH H HO H₂N HO- -H CHO -OH H HO- OH H- -H CH₂OH OHarrow_forwardThe structure of an unsaturated phospholipid is shown below. Which region of the molecule is most hydrophilic ? H₂N-CH₂ H₂C IV CH3 CH3 hydro-water philic-likes = Hydrophilic likes water ○ IV All regions are equally hydrophilic. IIIarrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
