(a)
Interpretation:
Line formula for 1-heptene has to be drawn.
Concept Introduction:
Organic compounds can be drawn from its IUPAC name. Initially, the parent chain is identified from the IUPAC name. After that the carbon chain is drawn with carbon atoms alone. Next step is to add the substituents in the respective positions as indicated in the IUPAC name. Remaining valency of carbon atom is satisfied by adding correct number of hydrogen atoms.
Line formula is the simplest representation of molecule. Carbon atoms are not explicitly shown in line formula. Intersection of lines and the end point of line are considered as carbon atoms. At the end-point it is understood as methyl group. Heteroatoms and hydrogen bonded to the heteroatoms are shown explicitly.
(b)
Interpretation:
Line formula for 2-heptene has to be drawn.
Concept Introduction:
Refer part (a).
(c)
Interpretation:
Line formula for 3-heptene has to be drawn.
Concept Introduction:
Refer part (a).
(d)
Interpretation:
Line formula for 2-methyl-2-hexene has to be drawn.
Concept Introduction:
Refer part (a).
(e)
Interpretation:
Line formula for 3-methyl-2-hexene has to be drawn.
Concept Introduction:
Refer part (a).
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Chapter 11 Solutions
GENERAL,ORGANIC,+BIOCHEMISTRY(LL)-PKG
- Draw structures corresponding to the following names and give IUPAC names for the following compounds: (8 Point) a) b) c) CH3 CH2CH3 CH3CHCH2CH2CH CH3 C=C H3C H H2C=C=CHCH3 d) CI e) (3E,5Z)-2,6-Dimethyl-1,3,5,7-octatetraene f) (Z)-4-bromo-3-methyl-3-penten-1-yne g) cis-1-Bromo-2-ethylcyclopentane h) (5R)-4,4,5-trichloro-3,3-dimethyldecanearrow_forwardNonearrow_forwardReview: Design a total total synthesis synthesis of the following compound using methyloxacyclopropane and any other necessary reagents.arrow_forward
- Nonearrow_forwardDraw a Newman projection from carbon 3 to carbon 2 in the highest energy conformation for the following molecule. What is this conformation called? What kind of strain is present? Brarrow_forwardWhich of the following dienophiles is most reactive in a Diels-Alder reaction: Please explain why the correct answer to this question is option 5. Please provide a detailed explanation.arrow_forward
- Which of the following would you expect to be aromatic? Please provide a detailed explanation.arrow_forwardDraw the enantiomer and diastereomers of the following molecule. Label each type of stereoisomers. Label each chiral center as R or S. HOarrow_forwardWhich diene and dienophile would you choose to synthesize the following compound? Please provide a detailed explanation. Please include a drawing showing the mechanism of the synthesis. Please also explain why it is the correct diene and dienophile.arrow_forward
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