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Q: 1. 2-chlorobutane 2. 1-butyne
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Q: Starting with 3-nitroaniline, show how to prepare the following compounds. Q.) 3-Bromoaniline
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Q: Starting with 3-nitroaniline, show how to prepare the following compounds. Q.) 3-Fluorophenol
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Starting with 3-nitroaniline, show how to prepare the following compounds.
Q.) 3-Fluoroaniline
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- Starting with 3-nitroaniline, show how to prepare the following compounds. Q.) 3-BromoanilineChoose exactly 3 answers from the choices 1. Nitrogen-containing functional groups: AmidesThiolsAzo dyesAmines 2. Carbonyl-containing functional groups: AldehydesEthersKetonesCarboxylic acids 3. Structural components/groups present in Ethoxymethane: Methyl groupEthyl groupOxygenEster linkageFollowing is the structural formula of the tranquilizer meparfynol (Oblivon). Propose a synthesis for this compound starting with acetylene and a ketone. (Notice the -yn- and -ol in the chemical name of this compound, indicating that it contains alkyne and hydroxyl functional groups.)
- Several diamines are building blocks for the synthesis of pharmaceuticals and agro-chemicals. Show how both 1,3-propanediamine and 1,4-butanediamine can be prepared from acrylonitrile.Give IUPAC names for the following compounds:Answers the following questions Q:1 Write the oxidation and reduction reactions of 3-methyl butanal. Q:2 Give one method to prepare propanone. Q:3 Give addition reaction of 2-propanol to propanone. Q:4 Give intermolecular hemiacetal of 6-chloro 4-ethyl 3-methyl 6-hydroxy 2-hexanone. Q:5 Give tautomer of 4-methyl 2-pentanone.
- Predict the products formed when cyclohexanone reacts with the following reagents. ) hydrazine, then hot, fused KOHDraw a structural formula for the product formed by treating butanal with reagent. Q.) LiAlH4 followed by H2O14. What is the IUPAC name for the following compound? NH- (a) propyl propanamide (b) propyl propanoate (c) N-propylptopanamine. (d) N, N-propylpropanamide (e) N-propxlpropanamide
- Provide the reagents for the reactions.When a compound like napihthalene C1oHa is dissolved in t-butyl methyl ether, then that solution is extracted with 3 M NaOH, and then the resulting basic aqueous layer is acidified with 6M HCI, what happens to the acidified aqueous layer? a) The naphthalene stays in the the aqueous layer as C10Ha O b) The naphthalene precipitates out as a solid, C10He O C) Nothing happens to the aqueous layer other than a dramatic raising of the pH d) The naphthalene stays in the aqueous layer as C10H>Na O e) Nothing happens to the aqueous layer other than a dramatic lowering of the pH O) The acid precipitates out as a solid, C10H>NaStarting with 1-butanol, select the reagents you would use to prepare the following compound: OH LiAlH4 followed by H3O+ Na2Cr₂O7, H₂SO4, H₂O NaBH4, MeOH O PCC, CH₂Cl₂