i would believe after many calculations the answer is 42
Name the carboxylic acid and the alcohol from which the folloving ester is derived. Write the...
Name the carboxylic acid and the alcohol from which the following ester is derived. Write the formal IUPAC name of the carboxylic acid and the alcohol in the corresponding boxes provided. Carboxylic Acid: Alcohol:
Question 1 The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol. H30*, H20 ? Provide an IUPAC name for the carboxylic acid that is produced. H BI U A A IX Ex'x, SE TTT12pt Paragraph The ester shown below undergoes hydrolysis to give a carboxylic acid and an alcohol. H30 H2O ? Provide an IUPAC name for the alcohol that is produced. HT BT U A T =
t-take&tak aldehyde pt ketone pt carboxylic acid "pt ester "pt amine "pt CH30 CH HO- Vanilin (Select all that apply) alcohol ether aldehyde ketone carboxylic acid ester amine 4 item attempts remaining SUB Try Another Version
Name the class of compound: COOH O Alcohol Aldehyde Carboxylic Acid Ester Ether O Ketone
Ketone alcohol alcohol alkyne aldehyde alkene amide amine Melatonin Bromatic Review Constanta Part A Give the IUPAC name of the ester shown. Carboxylic acid derivatives are organic compounds which the hydroxyl group of a carboxylic acid RCO-OH) is replaced with another group, such s an OR group (esters) or an-NH, NHR, + NR2 group (amides) determine the IUPAC name of an ester, follow he steps below 1. Name the R group of the COOR ester group as an alkyl group....
A Fischer Esterification reaction forms an ester from a carboxylic acid and an alcohol. This reaction is catalyzed with sulfuric acid (H2SO4). Which of the following statements below correctly describe an acid catalyzed reaction. Mark all the statements that are correct. Once the acid is consumed the reaction will stop until additional acid is added. An excess of acid is needed to get this reaction to run to completion. Acid is regenerated during the reaction. Only a small amount of...
(References) Name the carboxylic acid(s) with formula C H202 that contain two methyl branches on different carbons of the main chain. There are a maximum of 3 compounds that fit the description; if fewer than 3 compounds exist, leave the remainder of the spots blank. 1st compound: 2nd compound: 3rd compound: Submit Answer Try Another Version 1 Item attempt remaining
Part A CH, CH3 -CH=CH2-C-0-CH3 Enter the name of the carboxylic acid first, then the name of the alcohol. Separate the names 3-methyl butyric acid, methyl alcoh Submit Previous Answers Request Answer X Incorrect; Try Again Part B O O Enter the name of the carboxylic acid first, then the name of the alcohol. Separate the names wi benzenecarboxylic, ethanol Submit Previous Answers Request Answer X Incorrect; Try Again Part Type here to search o
write the con Chapter 16 Carboxylic Acids and Esters Name: 1) Write the condense structural formulas of the following compounds: Date: 3 methylpentanoic acid p-ethylbenzoic acid 4 m-hydroxylhexanoic acid 2) Which of the following compounds has the higher boiling point: butane, butanol, butanoic acid, and methyl ethanoate? Briefly explain why. 3) From the compounds of previous question, which is more soluble in water? Briefly explain why 4) Give the name of the carboxylic acid and alcohol used to prepare the...
and I A25). Name the ester prepared from ethanoic acid isobutyl alcohol? a. ethyl isobutyrate b. isobutyl ethanoate c. Butyl ethanoate dot-butyl ethanoate e. ethyl isobutanoate *26) organic carboxylic acids are: a. weak acids b. form Dimers d. a+b e. a+b+c c. have ka >