Please answer and explain reasoning and
methodology to achieve the answer.
Please answer and explain reasoning and methodology to achieve the answer. 1. (8 pts) Provide the...
Please answer and explain reasoning and
methodology to achieve the answer.
Br 2. (12 pts) For the reaction below, draw the product and show the mechanism as a catalytic cycle. Label each important step in the cycle, such as transmetallation, etc. Pd(PPh34 (5 mol %) -B(OH)2 THF/H20 K2CO3
Please answer and explain reasoning and
methodology to achieve the answer.
4. (6 pts) Give the metal's oxidation state for the metal compounds shown. O PPh Ni (t-BuzP)2Pd TiCl3 PPh3
Please answer and explain reasoning and
methodology to achieve the answer.
3. (6 pts) Provide the required starting materials for the synthesis of the desired product shown using a Suzuki coupling. You do NOT need to give the catalyst, solvent or reaction conditions. Suzuki coupling Oph Meo2c1 desired product
Please answer and explain reasoning and
methodology to achieve the answer.
5. (10 pts) Draw a chair transition state to explain the observed stereochemistry of the product. Provide a clear drawing for full credit. OLI THE. Он о Me Ph. HỒ Ph -78 °C | Phi Phi Me (+ enantiomer)
Please answer and explain
reasoning and methodology to achieve the answer.
e. (4 pts) Fill in the blanks: Mg M BETHF, 0 °C Me Si(t-Bu)CI EtzN, CH2Cl2 Grubbs' catalyst CH2Cl2, reflux
Predict the Product. (5 pts each; 20 pts TOTAL) Provide the stable organic product(s) that would result for each reaction below. Label the product formed in highest yield as “major" and include stereochemistry whenever appropriate. H20 (1 equiv.) HCI (catalytic) OH THF 65°C MgBr (2 equiv) 1-hydroxybutan-2-one Et20 25 °C Br2 (1 equiv.) benzene 80 °C UV light 2. NaOH H2O - THE 50 °C PCC 3. CH2Cl2 (1 equiv.) HCI (catalytic) benzaldehyde THF 65 °C mol. sieves
Please write the products you would get after each reagent is
added. Can you please show the mechanisms. Thank you
Acum Culi SO3 H2SO4 2 Br KMnO4 Br B(OH)2 Pd(PPh3)4, K2CO3 N toluene, heat + 1 equiv. Br2 light
What pdts would you expect from these rxns?
Determine which nitrogen atoms is basic. Explain the
answer!
a) 2 Culi SO3 H2SO4 Br KMnO4 Br B(OH)2 Pd(PPh3)4, K2CO3 b) 1 equiv. Br2 light toluene, heat N. N H
what bonds are made/broken in the palladium catalyzed reaction
of structure 8 and 9 shown below
and
what type if reaction occurs between 8 and 9?
Organic Letters Scheme 2. Total Synthesis of (---)-Aspergilazine A YNH Pd. (dba) (1 mol %) rac-BINAP (2 mol %) NaOBU (2.0 equiv) PhMe, 70 °C (75% yield) Br (1.0 equiv) (1.2 equiv) TES HN 9 (3 equiv) 0 1. Pd[P('Bu)gla (10 mol %) Cy2NMe, 1,4-dioxane, 80 °C (62% yield) 2. 1 N HCI/MeOH, 23...
Please predict the products of
the three reactions using the given catalyst, and explain the
reasoning and methodology to achieve the answer.
Me 0 Me / Me NUNTOMe Me ci Me Ru Ph ĐH cil РСуз Ru2, Grubbs' second generation catalyst d. (3 pts) Predict the products: Grubbs' cat. CH2Cl2, reflux Grubbs' cat. Heren CH2Cl2, reflux Grubbs' cat. OTMS rohetus CH2Cl2, reflux high dilution conditions