LiAlH4 reduce the Carboxylic acid into alcohol and Nitrile into amine.
Diazotization reaction followed by With CuBr gives alkyl bromide which undergo Elimination to 1-hexene.

[References] How would you synthesize the following compounds from butanoic acid using reagents from the table? Use letters from the table to list reagents in the order used (first at the left). Example: ab Reagents PBry I KOH / alcohol 1. NaBHA 2.H,0 KOB b .1. LIAH 2.HO f Mgidry ether HP 1.2. Cul 1.00, 2.,0* PE d 1-bromobutane HBr dark no peroxides NON 1.BH/THF 2 H2O. NaOH pt H.O heat 1 pt 1 pt a) octane g 1 pt...
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d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
if you were to heat pentanoic acid and 2 butanol with a strong acid you would most likely discover in your flask: A. a ketone B. an ester c. an amine d. an alkane e. an aldehyde explain please :)
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how you would synthesize the following acid using carbonation of a Grignard reagent.
How would you synthesize the following compounds from botanic acid using reagents from the table? Use letters from the table to list reagents in the order used (first at the left).
When the synthesis of this ester is attempted from the acid
(1-pentanoic acid), a second undesired molecule is isolated.
Provide the structure of the second molecule.
Ester:
What is the major product from a reaction of nitrobenzene with Fe/HCL? How would you synthesize 3-chlorobenzoic acid, starting with benzene?
Show how you would synthesize the following compounds
from 1-methylene cyclopentane
Q3. (i) Show how you would synthesize the following compounds from (Note; More than one step may be required) (8) - CH2 a). - NAPH NHPh
Pentanoic acid is primarily used for the synthesis of aromatic compounds of esters. A chemist wants to synthesize 2 Methyl Pentanoic acid in the laboratory. Discuss what could be the choice of the reactant that may lead to the synthesis of the desired product. Your answer must include four different steps (four different chemical reactions) leading to the synthesis of the desired product. All the organic compounds used/shown on the reaction must have a proper IUPAC name
How would you synthesize the following products? Thank
you!
Y 3. How would you synthesize the following products? Br HBK HC CH Br