Each of the following reactions has been reported in the chemical literature and gives a pre- dominance of a single product in synthetically acceptable yield. Write the structure of the prod- uct. Only monosubstitution is involved in each case, unless otherwise indicated. ***Draw the line structures in their entirety.*** C(CH3)3 CH(CH3)2 CH(CH3)2 NO₂ HNO, H₂SO₂ HNO, acetic acid

Each of the following reactions has been reported in the chemical literature and gives a pre- dominance of a single product in synthetically acceptable yield. Write the structure of the prod- uct. Only monosubstitution is involved in each case, unless otherwise indicated. Draw the line structures in their entirety. C(CH3)3 CH(CH3)2 CH(CH3)2 NO₂ HNO, H₂SO₂ HNO, acetic acid

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter21: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions

Section21.1: Naming Carboxylic Acid Derivatives

Problem 1P: Give IUPAC names for the following substances:

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Each of the following reactions has been reported in the chemical literature and gives a pre- dominance of a single product in synthetically acceptable yield. Write the structure of the prod- uct. Only monosubstitution is involved in each case, unless otherwise indicated. ***Draw the line structures in their entirety.*** C(CH3)3 CH(CH3)2 CH(CH3)2 NO₂ HNO, H₂SO4 HNO3 acetic acid
Give IUPAC names for the following substances:
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In an advanced synthetic chemistry experiment, a researcher prepares a compound, ZY-7, by reacting a ketone (C5H100) with hydroxylamine (NH2OH), followed by heating in the presence of an acid catalyst. The resulting compound, ZY-7, is then treated with a solution of sodium nitrite (NaNO2) and hydrochloric acid (HCI) at low temperature. Identify the class of compound that ZY-7 most likely belongs to after this series of reactions." A) Amide B) Oxime C) Nitro compound D) Diazonium salt E) Ester Don't use chatgpt please provide valuable answer
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An organic compound S reacted with ozone to give compounds Q and R. Both Q and R react with NaOH/I2 to produce a yellow precipitate with antiseptic smell. Q reacts with HCN to produce the compound CH3C(CH3)OHCN while R gives a silver mirror with Tollens reagent. I) write the structural formulae and names of Q,R,S and the Yellow Precipitate. II) write equations to show the reactions Q with NaOH/I2 and R with H^+/Cr2O7^2-
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Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. n-Pentanol (CH3CH2CH₂CH₂CH₂OH) and 2-methylbutan-2-ol (CH3CH₂C(CH3)2OH) are converted to their corresponding alkyl chorides on being reacted with hydrogen chloride. (a) Write out an equation for each reaction (b) Assign each the appropriate symbol (SN1 or SN2) (c) Write a suitable mechanism for each reaction
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Butene (CH2CHCH2CH3) reacts with hydrogen chloride (HCl) at room temperature. Draw the displayed formulae of the products formed in this reaction. State the name of the above reaction mechanism. Alkene Propene reacts with hydrogen bromide (HBr) at room temperature to produce, 1-bromopropane and 2-bromopropane. H2C=CHCH3 + HBr → CH2(Br)CH2CH3 + CH3CH(Br)CH3 Draw out the reaction mechanism of the reaction between propene and hydrogen bromide to produce 2-bromopropane. Use curly arrows to show the movement of electrons. The description should be detailed and must include the type of bond fission that takes place. You may sketch and insert suitable diagrams to aid your description if you wish. Referring to the above mechanism, explain why two products are formed…