QUESTION 5 Compound F is an ester that can be produced from the reaction between 2-methylpropanoyl chloride and ethanol. Compound F reacts with CH3CH(CH₂CH3)CH2OH produces Compound G and H. Compound F also undergoes reaction with (CH3)2NH to produce Compound P. Illustrate the chemical structures for Compound F, G, H and P.
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- Write equations for the reaction of 2-butanol with reagent. Where you predict no reaction, write NR. Q)K2Cr2O7, H2SO4, H2O, heatGive IUPAC names for the following substances:Prepare CH3COOC2H5, ethyl acetate, using ethyl alcohol. Write the chemical reaction. The pain reliever acetaminophen is produced by reacting 4-aminophenol with acetic anhydride. Outline a synthesis of acetaminophen from 4-aminophenol including any needed inorganic reagents.
- Question 6 (a) A cyclic, non-aromatic compound containing an attached carboxyl group is named by naming the cyclic compound exclusive of the -COOH group and then adding the suffix - carboxylic acid. Draw the structure of cis-2-methylcyclopentanecarboxylic acid. (b) A compound that contains both hydroxyl and carboxyl groups undergoes intramolecular ester formation. The product is called a lactone. Show the lactone formed from 5- hydroxypentanoic acid. (c) The structure below is pyrimidine. Draw the structure of purine. IyrimidineWrite the explicit structures of the following compounds. a) 2-methylbütannitril b) N-ethyl-N-methylmethanamite c) ethanoylpropanoate d) 3-methylanisol e) 3-ethylhexanedioic acidPredict the major organic product for the following reactions Draw the condensed structural formulas for the reactants and products and name the products (organic compounds only) If there is no reaction write NR. If a compound is a hemiacetal or acetal, don't name it – just label it as "hemiacetal" or “acctal." a) 2-methyl-3-pentanone + 2-propanol (isopropyl alcohol) b) Product in (a) + 2-butanol c) Complete oxidation of 3,4-dimethyl-1-pentanol (strong oxidizing agent) d) Hydration of 1,3-dimethylcyclopentene ) Intermolecular dehydration of 2-methyl-1-propanol (isobutyl alcohol)
- b) An alkyl halide W has the molecular formula CaH,Br. One of the isomers , X can rotate plane-polarised light . Another isomer, Y is a primary alkyl halide that reacts with ethanolic potassium hydroxide to form alkene, Z which can reacts with ozone and zinc followed by hydrolysis to yield propanone and methanal. Identify the compounds X. Y and Z.Click the "draw structure" button to launch the drawing utility. Draw the structure for the principal organic product formed in the reaction of 1-propanol with the following compound in the presence of pyridine. draw structure ... " I I I I I 1 H₂C -SO₂CI2. Write the structure for the most oxidized organic product when each of the following is reacted with potassium dichro- mate. Write NR if no reaction occurs.(a) methanol (b) ethyl alcohol (c) 2,3,4-trimethyl-2-pentanol (d) 3-hexanol 3. Alcohols can be made by reacting alkyl halides with sodium hydroxide as follows: RX +. NaOH ROH + NaX Give the names and formulas of the alcohols produced from the following alkyl bromides by this method:(a) 2-bromobutane(b) 2-bromo-3-ethylpentane (c) bromocyclopentane
- Question 2 (a) Give the reagents that are used to form the following products. RX Alkyl halides R- HO Carboxylic acid R- R' (D) Ketones (E) R R- OR' (В) (F) R Ester Alkenes ROH (A) (G) ROR' Ethers R H. Alcohols AldehydesIn 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 answer1. Esters can be formed by the condensation of a carboxylic acid with the hydroxyl group of an alcohol or phenol. a) Use structures to show the condensation of acetic acid (IUPAC: ethanoic acid) with the hydroxyl of cyclohexanol. b) Explain why 'condensation' is an appropriate name for this reaction. c) You'll synthesize the ester in aspirin by condensing the phenol group of salicylic acid not with acetic acid, but with acetic anhydride. Explain why the experiment calls for the use of an anhydride, rather than an acid.