Can you please explain the steps and products for:
Can you please explain the steps and products for: a) NaOH b) 1-bromopropane NH c) HCI,...
can you please show how eaxh reagent affects the starting
material to get to the product
1. EtMgBr, Et20 2. HBO NH a) NaOH b) 1-bromopropane c) HCI, H2O, A d) NaOH, H20 H₂N ONa ONa 1. DIBAL-H, -78 °C ОMe Et 2. MeOH, HCI Оме
35. Which of these is a weak base? A) NaOH C) NaCl B) HCI D) NH E) CH3CH2OH
Can you explain the mechanism?
CH3 Br, NaOH PhCH,-CH-CH,-C-NH,
Predict the products anticipated for the following reactions; 1. EtMgBr/THF 2. NH C/ H2O a. 1. n-BuLi, Et2O 2. NH CI, H2O b. H KCN, HCI C. NaCN, HC d.
Complete the following reations : A. H2O + H2O B. HCI + H2O C. NAOH + H2O D. NH40H + H2O E. H2SO4 + H2O F. CH3COOH + H2O 1. If the pH of NaOH is 12.7, what is its concentration? 2. If the pOH of HCI is 12.7, what is its concentration?
NaOH B. H2O CHÚNH + CO2 H₃C NH₂ Amides can be converted into primary amines with the loss of a single carbon atom by the Hofmann rearrangement. The reactson involves treating a primary amide with Br, and base Draw curved arrows to show the movement of electrons in this step of the mechanism Arrow paling Instructions nn OH НС :: H3C-NH, OH CO, H2O H-OH
Can you please show the product and the steps for:
1. LiAIHA ОMe 2. acetone, HCI
products?
NaOH, A Na2Cr2O H2SO4, H20 NaBH HCI 0°C NO2 Ph.P H3C Na, MeOH H2SO4, H20 NH, 1HỶ, HCN 2. H30*, A
Select the major product of the following reaction scheme: Reaction NaOH HCI NH2 H2O 25°C 100°C A D NH2 OH B E co -NH F NH2 NH2 (No Reaction) Ol. A OII. B oll. O IV.D OV. E OVLF
a. HCI O C Br2 0°C Δ OH NaOH, heat NaOH он X. 1. LDA O 2 3. H2O