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 functional group. The prefix with locant number indicates the number of substituents and their respective position at the main chain or a ring of carbon atoms.
(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 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 a ring of carbon atoms.
(d)
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 a ring of carbon atoms.
The stereochemical designation and the locators are enclosed in paranthesis 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
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Chapter E Solutions
ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
- Give the appropriate/simplest IUPAC name of the compound (see attached picture) A.) 1,3-dimethyl-2-oxo-cyclopentane-1-carbaldehyde B.) 1,3-dimethyl-2-oxo-cyclopetane-3-carbaldehyde C.) 2,5-dimethyl-2-carbaldehyde-cyclopentanone D.) 2,5-dimethyl-2-carbonyl-cyclopentanone E.) 2,5-dimethyl-2-methaldehyde-cyclopentanonearrow_forwardhi! i need answers on letters d to f. The instructions says give the IUPAC name of each compound. Thank u!arrow_forwardLabel each of the following structures as a cyclic hemiacetal, hemiketal, acetal, ketal, or none of these: a. b. c.arrow_forward
- Give the IUPAC name for each compound (a)-(e)arrow_forwardAnswer each question using the ball-and-stick model of compound A. Draw a stereoisomer for A and give its IUPAC name.Draw a constitutional isomer that contains an OH group and give itsIUPAC name.arrow_forwardAnswer each question using the ball-and-stick model of compound A.a.Give the IUPAC name for A, including R,S designations for stereogenic centers. b.Classify A as a 1°, 2°, or 3° alcohol. c.Draw a stereoisomer for A and give its IUPAC name. d.Draw a constitutional isomer that contains an OH group and give its IUPAC name. e.Draw a constitutional isomer that contains an ether and give its IUPAC name. f.Draw the products formed (including stereochemistry) when A is treated with each reagent: [1] NaH; [2] H2SO4; [3] POCl3, pyridine; [4] HCl; [5] SOCl2, pyridine; [6] TsCl, pyridinearrow_forward
- A is a toxin produced by the poisonous seaweed Chlorodesmis fastigiata. (a) Label each alkene that exhibits stereoisomerism as E or Z.arrow_forwardDraw the missing starting material. Reagent 1 is benzene and AlCl3. Reagent B is Zn(Hg) and HCl.arrow_forwardIdentify the IUPAC name of the given structure. A. 2 - methylhexan-5-one B. 5 - methylhexan-2-one C. 2 - heptanone D. 5 - heptanone Identify the IUPAC name of the given structure. A. 4 - bromopentan-3-one B. 1 - bromobutan-2-one C. 2 - bromobutan-one D. None of the abovearrow_forward
- Give the IUPAC or common name for each compound. (A - E)arrow_forwardWhich has a higher boiling point and indicates the most important reason. Circle the compound with the higher boiling point. Reason KBr vs. CH3CH2Br CH3CH(OH)CH3 vs. CH3OCH2CH3arrow_forwardDraw the structure corresponding to each IUPAC namearrow_forward
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