Concept explainers
(a)
Interpretation:
The structure from the given IUPAC name is to be drawn.
Concept introduction:
The root name in the given IUPAC name suggests the main chain or ring of carbon atoms in the compound. The suffix to root name indicates the highest priority
Suffix ‘oate’ represents ester as the highest priority group and the prefix in the IUPAC name is the group attached to O atom.
(b)
Interpretation:
The structure from the given IUPAC name is to be drawn.
Concept introduction:
The root name in the given IUPAC name suggests the main chain or ring of carbon atoms in the compound. The suffix to root name indicates the highest priority functional group. The prefix with locant number indicates the number of substituents and their respective position at the main chain or at a ring of carbon atoms.
(c)
Interpretation:
The structure from the given IUPAC name is to be drawn.
Concept introduction:
The root name in the given IUPAC name suggests the main chain or ring of carbon atoms in the compound. The suffix to root name indicates the highest priority functional group. The prefix with locant number indicates the number of substituents and their respective position at the main chain or at a ring of carbon atoms.
(d)
Interpretation:
The structure from the given IUPAC name is to be drawn.
Concept introduction:
The root name in the given IUPAC name suggests the main chain or ring of carbon atoms in the compound. The suffix to root name indicates the highest priority functional group. The prefix with locant number indicates the number of substituents and their respective position at the main chain or at a ring of carbon atoms.
(e)
Interpretation:
The structure from the given IUPAC name with appropriate stereochemistry is to be drawn.
Concept introduction:
The root name in the given IUPAC name suggests the main chain or ring of carbon atoms in the compound. The suffix to root name indicates the highest priority functional group. The prefix with locant number indicates the number of substituents and their respective position at the main chain or at a ring of carbon atoms.
The stereochemical designation and the locators are enclosed in parenthesis at the very beginning of the name. The stereochemistry at the chiral center is determined by assigning the priorities to the groups attached to chiral center on the basis of the

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Chapter F Solutions
ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
- Which 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_forwardPredict the product of the following reactions: O 0= excess Х Кон ОН H+ H+ Iarrow_forwardHow many chiral centers/stereocenters are there in the following molecule? 1 2 3 4arrow_forward
- Which of these correspond to the molecule: 2,5-dimethylheptanearrow_forwardGiven 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_forward
- The 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_forwardWhich of the following compounds would you most appropriately call hydrophobic? ○ CH4 H2CO CO HCI ○ NaClarrow_forwardWhich of the following triglycerides would you most expect to be a liquid at room temperature? saturated fat trans monounsaturated fat trans polyunsaturated fat cis monounsaturated fat ○ cis polyunsaturated fatarrow_forward
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