1. H2SO4 acts as strong oxidizing agent in addition to as dehydrating reagent hence H3PO4 is better reagent for dehydration of alcohol and it is dafer over H2SO4.
3. Sicne HCl causes the formation of dubstisubst product instead elimination product.
4. To remove the the formed water as salting out.
worksheet torcyclohexene" 1. Why do we use H3PO4 instead of H2SO4 as a catalyst for the...
2. Why do we use H3PO4 instead of HCl as a catalyst for the synthesis of cyclohexene? (3 pts.)
In the process of the purification of cyclohexene, we used a saturated NaCl solution to wash the crude product instead of the same volume of pure water. Explain why.
when computing the cross product why do we use a -j instead of j?
QUESTIONS 1. What is the purpose of the sulfuric acid (yes, it's a catalyst, but why is it a catalyst? What is it doing that makes the reaction possible? Would the reaction just go slower without it, or would the reaction not go at all? Why?) 2. If isobutyl alcohol (2 methyl propanol) is used instead of tert butyl alcohol, a mixture of products is obtained. One the products is the same as the product obtained with the tert butyl...
1) Why do we use a mixture of ethyl acetate and hexanes as solvents in the synthesis of 5,6-endo-dicarboxylic anhydride? 2) What do the terms exo and endo refer to? 3) Why do we not do any TLC on the product in the synthesis of 5,6-endo-dicarboxylic anhydride?
Working on the questions at the end of this lab report (see above). I need help answering questions 2, 3, and 4 completely and thoroughly. Thank you! s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
7) Name four reagents you can use to dry solvent. Why do we use magnesium sulfate in this lab instead of them? Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via nucleophilic substitution. In this type of reaction, the nucleophile displaces a leaving group from a carbon atom of an organic substrate (here the alcohol once protonated). Both electrons of the new bond to the carbon are provided by the nucleophile...
Please explain what is going on in this lab for STEP 3. what are some important factors? Multistep Synthesis Preparation of 4,4-Diphenyl-3-buten-2-one! This experiment illustrates se multistep synthesis, in which the the next. This process is very common iment illustrates several important concepts of organic synthesis. It is a synthesis, in which the product of one reaction becomes the starting material of This process is very common in industry and research, and demands careful to vields and techniques. The experiment...