Need help with both questions Terminal alkynes react with bromine and water to give bromoketones for...
(b) Alkynes react with aqueous sulfuric acid, in the presence of catalytic Hg2+ salts, to give aldehydes or ketones. Consider the following reaction. H H 2SO4/H2O / HgSO4 H2C-C-CEC-H ketone (i) Show the structure of the product (2 marks) (ii) Give the mechanism for its formation.
3. Give the detailed mechanism of the following reaction and name the amide and the products: - Br КОН ethanol-water, heat OK + H2N- 4. Synthesize the following compound by using a nitrile and a Grignard reagent. You need to show the synthesis of the nitrile and Grignard reagent. 5. Propose a scheme for synthesizing the following compound using methyl cyclopentanecarboxylate, iodomethane and other reagents : -OH
Questions are a continuation of questions 2,3. Thank you for you
help! I really need help with just 3&4.
3.Suppose you wish to perform the reation you wrote in
problem 2 on the other -OH group.How might you prepare the molecule
in order to do so? Suggest appropiate reagents and draw your
expected products.
4. Suppose after your preparation performed in problem
3, the molecule reacts very slowly with HBr. How could you prepare
the -OH group you want to...
Whats the mechanism of this reaction to give
quinine
Problem 4: (10pts) Suggest a reasonable chemical mechanism synthesis of alkaloids Quinine and give a chemical structure of Compounds A, B, C, D, E according the following reaction scheme: Pr,NC H.so THF NaBH, Bu AlH Ba(OH)2 OH (-)-Quinine
need help with both questions.
4. Show the structure at the end of each step in the following reaction sequence. The first step is a Claison reaction. 3) 1.NaOCH 2. H30. Heat 3. Heat Eto Et 5. (From last exam)Predict the organic products of and show the mechanism of the following reaction. H30*
if someone could please help me with this
8. Give the alkene you would need to make each the following compounds (6 points, 2 each) 9. Propose a mechanism for the following reaction. Be sure to show the flow of electrons and the structure of any reactive intermediate (6 points)
please need help with a-f
ADDITIONAL PROBLEMS Naming Alkynes 9-26 Give IUPAC names for the following compounds: (b) CH3C CCH2CECCH2CH3 CHз (a) CHзCH2сCCCHнз CHз (d) CH3 CH3 CHз (c) HC CCCH2CCH CH3CH=CC CHCH3 4 CHз CH2CH3 (e) H2C=CHCH=CHC= CH (f) CH3CH2CHC CCHCHCH3 CH-CHз CHз
Need help with questions 2-4.
Information: Just as it is beneficial to make a summary of the types of reactions, it is a list of the functional groups that commonly react by each of the Seven summary is shown in Table 2. is also useful to the ven pathways. Such reaction pathways Table 2: Functional groups that commonly react by the seven react acid-base - carboxylic acids, phenols (acids) - amines (bases) addition - alkenes, alkynes elimination - alcohols reduction...
6. a) Hydrogen and carbon monoxide react to give formaldehyde under certain conditions. The reacti on scheme below is the proposed mechanism. Verify that the scheme is correct and derive the rate law (equation) for the reaction. H2 2H k2 fast (reversible equilibrium) H HCO HCHo ....fast b) Write down the rate law (equation) for each of the following if each is an elementary reaction. Write down also the molecularity of the reaction i) 2NO + O2- > 2 NO2...
1. Given the following structures that react by Sn1, which would react fastest and which would react slowest. Give reasoning. 5-bromo-1,3-pentadiene, bromocyclopentane, (R)-2-bromo-2-methylhexane. 2.If bromocyclohexane reacts faster than chlorocyclohexane in an Sn2 reaction, what could be the reason? 3.You wish to substitute the bromine in the following molecules with a nucleophile. Explain whether the given molecule would react by Sn1 or Sn2 mechanism and explain why. 1-methyl-1-bromo-cyclohexane, 1-bromopropane, 2-bromohexane. 4. Why does benzyl bromide react under both Sn1 and Sn2...