Could you please answer questions 2-5 2. Complete the following reactions by writing the missing reagents...
Draw a multistep synthetic route to accomplish the following transformation. Please explain! 4. Draw a multistep synthetic route to accomplish the following transformation (8 points) COOH - - - &
Complete the following questions/reactions by providing the missing portions shown by empty boxes. In some cases, not all boxes may be used or necessary. Show all major organic products unless otherwise specified. Make sure to clearly indicate stereochemistry where necessary. 1) CH, 2) H0* H O OH OH HCI NaOH но HO HC OH MgBr 1) THE 2) acid CH, HO Brg
Please help me solve this urgently Accomplish the following reactions. CH3Ch2OCHO + CH:"CHCH,MgBr. , 2. (18%) (1) ether (1) (2)H1,0 BH THF HO(3) NaBH) OH
Complete the following questions/reactions by providing the missing portions shown by empty boxes. In some cases, not all boxes may be used or necessary. Show all major organic products unless otherwise specified. Make sure to clearly indicate stereochemistry where necessary CH, OH OH OH Br MgBr OH но CH, C AICI, KMnO4, H2O HC heat CHE 6363638 (CH,CH, Culi
Which reagents would best accomplish the following transformation? ОН N 1. Potassium Phthalimide 2. CH3NH2 3. N2H4 O 1. CH3NH2 2. LiAlH4 3. H30+ O 1. SOCl2, pyridine 2. CH3NH2 O 1. p-TsOH, HOCH CHOH 2. CH3NH2 3. H30+ ? 3:13 PM 7/30/2020 Which reaction sequence would accomplish this transformation? oth HO H O 1. CH3MgBr 2. H30+ 3. CH3OH 1. H30+, CH3OH 2. NaBH4 3. H30+ O 1. p-TOH, HOCH CH2OH 2. NaBH: 3. H30+ O 1. pTSOH, HOCH,CH,OH...
1. Give a sequence of reactions to accomplish the following transformation? Show mechanism 2. What reagent(s) would accomplish the following? Show mechanism. R-CH2-NH2 R-C-NH2 3. What would result from the reactions shown below? Hsco-s-OCH3 large excess) NaOH нон H,0 но ОН "ОН (a and B) 4. Predict the major product of the following reaction. CHNNH 3 equivalents) но CHCH2OH Heat он CH2OH Draw the Haworth projection for chair conformation of a-D-Glucopyranose (shown below) CH2OH HO H OH OH
Im stuck on these, can you please help me? thank you :) 1. 2. 3. 4. Predict the product from the following sequence (the reagent over the first arrow from the left is hydroxide, the minus charge on OH may not be showing clearly): i 1 point: Сн Y но be (0) NOR CHOH 2 gi EI HO OH ON OAV Ос. II OD 1 E. IV Question 2 Predict the product from the following sequence (the reagent over the...
please do both problems 1&2 Predict the major product of each of the following reactions. MgBr 1. CH LI? CN 2. CH,OH 1. CH L ? 2. Н,оо ? 2. Н,о0 (c) (a) (b) Draw the mechanism and predict the major product for each of the following reactions. 2 (b) (c) 1. КCN, HO, ? 2. H2SO 1. KCN, H,O 1. CH,MgBr, ether ? 2. HaSO 2. H,O (e) CH,CH,SNa? CuLi ? 2. H,O Ethanol
14. (4 points each) Complete the following reactions showing the major organic product). 2 CH,NH CH CH,OH Ci pyridine 2. 2CH,NH2 Ci AICl I. excess CH,MgBr 2. H CH,CH,CH OH NaOH 14. (4 points each) Complete the following reactions showing the major organic product). 2 CH,NH CH CH,OH Ci pyridine 2. 2CH,NH2 Ci AICl I. excess CH,MgBr 2. H CH,CH,CH OH NaOH
Organic Chemistry please help asap 70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...