View Policies Current Attemptin Progress (+)-Citronellal is the main compound responsible for the lemon scent of citronella oil. In addition to its well-known insect repellant properties, it also has some antifungal properties. (+)-Citronellal also has been used as a starting material to make compound 1. (+ Chronetlal Provide an IUPAC name for compound 1. Note that the name must include a stereodescriptor (R or S) to iddntify the configuration of the chiral center.

View Policies Current Attemptin Progress (+)-Citronellal is the main compound responsible for the lemon scent of citronella oil. In addition to its well-known insect repellant properties, it also has some antifungal properties. (+)-Citronellal also has been used as a starting material to make compound 1. (+ Chronetlal Provide an IUPAC name for compound 1. Note that the name must include a stereodescriptor (R or S) to iddntify the configuration of the chiral center.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter23: Amines

Section: Chapter Questions

Problem 23.67P

See similar textbooks

Similar questions

Provide the IUPAC name for the following carbonyl compounds?
Answer the following Compounds CORRECTLY by giving the IUPAC NAME OF IT.•Label with proper notations (like hyphen, commas, periods, and grouping symbols) thank u❤️
Give the IUPAC name for the following compound
Phenylethanol can be oxidised to phenylethanal or phenylethanoic acid, depending on the reagents used (both the alcohol and the aldehyde are of interest for their antimicrobial properties, while the acid is used to treat type II hyperammonemia): A (a) (b) (c) CoH,CH,CHO phenylethanal B C6H5CH₂CH₂OHC₂H₂CH₂CO₂H phenylethanol Suggest reagents (shown as A and B in the scheme above) that could be used to carry out the oxidation of the alcohol to the aldehyde and the acid, respectively. C6H5CH₂- Suggest two other syntheses of phenylethanoic acid, in each case indicating the starting materials and other reagents required, but not giving details of mechanism. One of your proposed syntheses must start with a compound which only contains seven carbon atoms (the acid product contains eight carbon atoms). phenylethanoic acid Phenylethanal can be converted to a hydrate in the presence of aqueous acid, though the position of equilibrium is very far to the left: H H+/H₂O OH C6H5CH₂-C-H OH Explain why…
Give the IUPAC names (including E,Z and R,S designations).
Compound 1 is an anticoagulant that is extracted from, among other plants, the sweetclover plant, Melilotus Officinalis. However, the compound is moderately toxic and alsofinds use as a rodenticide. Name this compound
c) rite in the reagent(s) over the arrow. a) C6H5N₂+ b) C6H5C=N H3C- An OH H₂C → benzene H3C benzylamine CI CH3
Give the IUPAC name for each compound, including any R,S designation.
Pick the best IUPAC name for the following molecule: CH3 CH3 CH3 2-methoxy-6-ethylheptanal 2-methoxy-6-methylactanal O 2-ethyl-6-methoxyheptanal O 6-ethyl-2-ethylheptanal tm
which of the foolowing Compounds whose structure/s involve a benzene ring and two substituents o-cresol 2-bromophenol cathecol m-cresol resorcinol phenol
should not be classified as an acetal?
2) Provide an acceptable name for the compound below. OH CH₂CH₂CH3 106 gaidie than methanol Use appropriate