mechanism for hexamethylenetetramine (CH, (NH) + 6 HO Hexamethylenetetramine (CH, MN ) Water (HO)
d Geminal disor inches of water e water to recarbonyl and alchydes Propose a mechanism for the HO OH CH ---CH prope 2.2. = CH-C-CH - HD
NH .CH HO H.CO (d)
1) Provide structures for A-J in the following roadmap. H NaN CH,NH LAIRL CH,OH (XS) CH,OH SOCI, E A B D Fr, Cafe 1) KOH, HO 2) H0 NH, SOCI: 2) Propose a mechanism for the following transformation, including arrows to describe electron flow, and all intermediates. NaOH HO OH
6. The structure of 2-ethylbenzamide is C-NH CH-CH3 C-NH-CH-CH NH-CH O CH,-CH C-NH2 do CH-CH:
Mechanism Proposal CH, HO Snci, -OCH -CH(OCH3)2
Can you explain the mechanism? CH3 Br, NaOH PhCH,-CH-CH,-C-NH,
formulate a mechanism for the following problem. 3. Formulate a mechanism for the formulation of acetamide,CH-CO-NH,, from methyl acetate and ammonia.
Please help. Thank you HgC OH HỌC HO-NH₂ a CH₂ HyCN III H₃C N CH₂. CH, IV OBO CH: H₂C – NH₃ سان. ولی من H₃C N H3C CH₂ OH HACO H3C 2-2 | لا اله What is the expected product when a sample of succinc acid is heated? OH Heat e AO 1. H,O, HCI, heat 2. SOCI, pyridine (a base) CEN NH CI TV OBOS Trper to
1. From the following reaction, CH,6:9 HO – CH3OH + Họ methoxide water methanol hydroxide a. choose the Bronsted-Lowry base and its conjugate acid b. choose the Bronsted-Lowry acid and its conjugate base 2. What is/are the product(s) of the following reaction? 3. Identify the most acidic and least acidic protons in this organic compound. 4. For the following pairs, choose the strongest acid: a. HgS* vs H:S b. H2S vs H Se H₂C=NH2 HC=NH (6) 1 5. For each...
Propose a mechanism from the reaction in the box CH,CH,0 + NH CH:CH-OH + NH3 Use the diagram above for Questions 4-7. 4. Which reactant is the base? a) CH3CH20 b) NHÀ c.) CH,CHOH d.) NH3 5. Which product is the conjugate acid? a.) CH CH20 b.) NH4+ c.) CHCH2OH d.) NH3 6. Which reactant is the acid? a.) CH,CH20 b.) NHÀ c.) CH3CH2OH d.) NHS 7. Which product is the conjugate base? a.) CH,CH20 b) NH4* c.) CH,CH2OH d)...