Show how you could prepare each of the following carboxylic acids using Grignard's reagent: OH from...
using reagents and necessary solvents, show how you would convert the molecule given into the producta shown. number of steps auggested to take are above the arrow H2U y moving OEC ) remat Lg. -0 2-methylbut-2-enemy W O H259, R 1. 3-methylbut-1-ene onal group wrangement. LOH N 3. i 3 2 2,3-dimethylbut-1-ane 1-chloropropane propyne Hofman Meedbury Oxymercirono dimere or 115/ year ang puke Jonats but-1-ene oup opalkene 5 new posinan cis-pent-2-ene 6. pent-2-yne trans-pent-2-ene 7. 3-methyl-1-chlorobutane OH 2-methylpent-1-ene trans-hex-2-ene propyne...
We made esters from carboxylic acids and alcohol. (for one of them, acetic acid + isopentyl alcohol + couple drops of sulfuric acid). Could someone please explain those. Thank you 1. Consider if we had prepared high molecular weight esters, what problems would this pose regarding our method of analysis 2. We used sulfuric acid as a catalyst, but carboxylic acids are a reagent in this reaction. Would simply using excess carboxylic acid work as efficiently as sulfuric acid to...
Instead of propanoic acid, show using propanol please 5. Synthesis: Show how the amine could be prepared from benzene, propanoic acid and dimethyl amine. More than one synthetic transformation will be necessary. You have unlimited access to any inorganic reagent. ОН and and
Part 1: Carboxylic Acids and their derivatives 1. Complete the following synthesis by addingthe appropriate reagent(s) (4 points Et Reagent(s) A Reagent(s)B 2 Oomplete the following synthesis by adding the appropriate reagent(s). (4 points Reagent(s) A Reagent(s) B 3. Complete the following synthesis by adingthe appropriate reagent(s). (4 points) он Reagent(s)A Reagent(s) B Page 1 of 13
Show how to prepare the following from a carboxylic acid and a 2nd compound Show how to prepare the following from a carboxylic acid and a 2nd compound * CH, COCH,CH, CH, CH, CH,CH,CH, CÁCH « CH,CH. ENHCH
Please help with study pack. Thank you! What reagent could be used to carry out each of the following steps? Anwer 3. ? Answer 3/5 a. Toluene …→ benzoic acid -..........→ benzyl alcohol → benzaldehyde b. benzaldehyde →styrene → (1-hydroxyethyl)benzene → isopropylbenzene (1-hydroxyethyljbenzene-…__→acetophenone c. → (1-methylethenyl)benzene ー→ d. Isopropylbenz ene → ethylbenzene (1-methyletherylbendzene__→ acetophenone-_ e. 0g
1. Naming and Drawing Carboxylic Acids: 1.A. Using IUPAC guidelines, enter the name for the carboxylic acid shown below. Enter the name using IUPAC guidelines, including numbers and punctuation (e.g., 3,4-dichlorobenzoic acid). 1.B. Draw 3-methylbenzoic acid. (Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Include all hydrogen atoms). 2. Naming Carboxylic Acid Derivatives: 2.A. Give the IUPAC name of the ester shown....
Devise a 5-step synthesis of the carboxylic acid from acetylene. 1. reagent 1 2. reagent 2 3. reagent 3 ОН H-C=CH H3C1 4. reagent 4 5. reagent 5
write a chemical reaction for each esterification using the line angle formulas of the carboxylic acids and alcohols listed in table 1: (1-5) Table 1. Preparation guidelines for part 2 esterification reactions. test tube number carboxylic acid alcohol тон H OH formic acid isobutyl alcohol OH OH acetic acid benzyl alcohol OH acetic acid OH Isopentyl alcohol OH ethyl alcohol OH acetic acid OH -OH methyl alcohol Гон salicylic acid
help with all of them please 1) Complete the following reactions OH H2SO4 (a) (b) OH H2SO4 (c) H2SO4 heat heat OH heat ОН H.CO d) HỌCrO, H2C104 e) -OH OH 2) Show how to convert (a) 1-Propanol to 2-propanol in two steps (b) Cyclohexene to cyclohexanone in two steps (c) Propene to propanone (acetone) in two steps. 3) Write a stepwise mechanism for the sulfonation of benzene. Use HSO3 + as the electrophile.