Question 10 ( Show how you would make the target componds on the right from the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms. (土) OH
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- In each reaction box, place the best reagent and conditions from the list.Please explain the chosen letter. In the sequence of reactions below, A and B are which of the following? o NaCN, (HCl) H3O+ →B (CH3),CO- A- A а. (CН3)2C(ОН)CN, (CH3)2C(ОH)соон b. (CH3)2C(ОН)CN, (CH3)2C (ОН)2 с. (CНз)2C(ОH)CN, (CH3)2CHCOОН d. (CH3)2C(OH)CN, (CH3)2C=OWhat is the correct sequence of steps for the following transformation? Step 1 Step 2 HO (a) HBr, followed by H20 (b) H2 over Lindlar's catalyst, followed by H2O/H,SO4 (c) H2O/H2SO4/H&SO4, followed by HBr (d) H2 over Pd/C, followed by H20 Which structure corresponds to the missing step in the reaction mechanism for the conversion of the alkene/alcohol to the cyclic ether? HC! H20 + H;O OH OH OH (a) (b) (c) (d)
- Complete the synthesis of the following compound from the starting material given (2- oxocyclohexane-1-carbaldehyde). Over/next to the reaction arrows, list out all reagents/solvents used. Draw intermediate structures in the boxes. You may use as many steps as you think necessary. You do NOT have to draw the mechanisms.Cro3, H30* (CH5)3P*_-CH2, THE CH;CH2CH2OH CH3CH2CH CH;CH,CH=CH2 a b This reaction scheme is flawed; the reagents shown for reactions 'a' and 'b' may or may not be correct. Choose the correct reaction conditions for these two reactions from the table provided. Enter your choices as a simple 2 letter string, i.e. without spaces or punctuation. Correct reagents a. CH3 MgBr then H3O+ e. Periodinane, CH2 Cl2 b. CrOз, HзО* f. LIAIH4 then H2O c. H3 O+ g. H2NNH2, KОН d. Li(CH3)2 Cu then H3 O* h. The given reagent is correctPlease help me with both of these problems, they are the same question its just a two-part, I really want to study so please help
- Explain the mechanism and show the steps6. The following reaction is an example of OH A) SN1 B) SN2 Br NaOH EtOH C) E1 D) E2 7. In the above reaction (Q6), what is the role of NaOH? A) It acts as an acid and reacts with EtOH B) It acts as nucleophile and attacks on electrophilic carbon in bromoprop C) It acts as a base and reacts with phenolic OH and forms phenolate ion D) It acts as a spectatora) Briefly explain the reason by showing what kind of reaction mechanism the main product (major) and by-product (minor) will be formed as a result of the reaction of 1 chlorobutane and 2 chloro butane with NaOH, a strong base (nucleophile). b) In the presence of a polar solvent and in the presence of a polar solvent and reacting with sodium ethoxide (NaOC,H5), 2-Bromo-2-methyl propane can be formed when the main product (major) and by-product (minor) will be formed by showing which reaction mechanism will be followed and briefly explain why.
- Propose a mechanism for the conjugate addition of a nucleophile ( Nuc:" ) to acrylonitrile ( CH,=CHCN ). Use resonance forms to show how the cyano group activates the double bond for conjugate addition.Which reagent/catalyst would be expected to bring about the following conversion? OH CH;CH2CH,CH CH;CH2CH,C-H ÓCH, Ag(NH3)2" / OH CH3OH / H3O* (1) NaBH4 (2) H30* O HNO3 / H2SO4 O K2Cr207/ H2SO4Predict the product and draw the mechanism of its formation. Include lone pairs and charges in your answer. Using wedges and dashes to indicate the stereochemistry as necessary. Do not use abbreviations such as Me or Ph in your drawings. Do not explicitly draw any hydrogen atoms in any of your products. & Me 13.16d1 1) LIAIH. 2) H₂O Draw the first step of the mechanism (Use H as the nucleophile). CH, +H Edit Drawing