l. First Cl is replaced with N3 which is reduced to NH2.
m. Micheal addition
n.Hoffmann exhaustive methylation followed by elimination to give 1- alkene
o. diazocoupling
p. Sandmeyer reaction
q. diazotisation follwed by removal of nitrogen
g. intramolecular aldol condensation
I need all asap plesse ON 1. NaN3 2. LiAIH4 3.Hzo NaOEt, heat 1.xs CH31 2....
Write the products of these reactions
-NH2 1. NaNO2, HCI 2. CuCN 1. N(CH3)3 2. Ag20, H20 3.A 1. LAIHA 2. H20 NaN3 1. LATHA 2. H2O NaCN 1. LIAH 2. H20 Br NaCN H. Ni HNO3 H2SO4 NaOH H20 1. NaNO2 HCI 2. HBF 4 CH3 HNO3 Na Cr207 H2SO4 H2SO4 Sn HCI 1. NaNO2 HCI 2. CuCN
Draw the major product for each reaction. он. CH3 heat N(CH3)3 a. LiAIH4, Et20 b. H30*/H20 1. NaCN, DMSO Br 2. a. LiAIH4. THF b. H3O+/H2O 1. NaN3, DMSO Br 2. a. LiAIH4, THF b. H3O /H20 1. HNO3, H2SO4 2. SnCl2 3. Br2 4. a. HNO2, H2SO4 H3C b. H2PO2 NH2 1. NaNO2, HCI, H20 но 2. HBF4
What are the steps that give this product given the reagent
list.
Multistop Synthesis NH₂ A. Cl2/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO2/HCI E. HC1/Cuci F, KCN/CuCN G. H3PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H20 K. H/Ni L. 1) Mg 2)CO2 3)H30 M. CH3OH/H30* N. (CH3)2SO4 NaOH 0. CH3OH P. SOCl2 Q. HC1 R. NaN3
Using the reagents listed below, propose a synthesis of the target compound starting from benzene. Assume all reactions are appropriately worked up and that mixture of constitutional isomers can be separated. CI NH2 A. Cl/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO2/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H Cr04 J. 1)LiAlH4 2)H20 K. H/Ni L. 1) Mg 2)CO2 3)H30 M. CH3OH/H30+ N. (CH3)2SO4 NaOH O. CH3OH SOCI Q. HCI R. NaN3
Synthesis of target compound starting from benzene. Assume all
reactions are appropriately worked up and that mixtures of
constitutional isomers can be separated. May use a reagent more
than once if needed.
A. Cly/FeCl3 B. HNO3/H2SO4 C. CH3COCI/AICI: D. NaNO/HCI E. HC1/Cuci F. KCN/CuCN G. H3PO2 H. H2O/heat I. H2Cr04 J. 1)LiAlH42)H2O K. H/Ni L. 1) Mg 2)CO2 3)H30* M. CH3OH/H30* N. (CH3)2SO4 NaOH 0. CH3OH P. SOCl2 Q. HC1 R. NaN3 -NH₂ CI
1. Predict the major product for the reactions shown below; pick any 5: HO xs CHal Ag20 NaOEt EtOH, Δ -H2O HO но он 0 он H2SO4 H20, A heat 1) PhMgBr 1) NaOH, Br2 2) 5% HCI 2)H3O+, Δ OEt 1) PPh3 3) KOtBu 2) O 1) NaOH on. Br 2) O o
1. Predict the major product for the reactions shown below; pick any 5: HO xs CHal Ag20 NaOEt EtOH, Δ -H2O HO но он 0 он...
D 1) SOCI2. py OH 2) NaCN What is the major product of the above reaction sequence? IN CN CI CI CN NH2 1) CHI (xs) 2) Ag20 3) A What is the major product of the reaction? NH2 ON + NaOH NOZ What is the major product of the above reaction? ON OH NOZ ON OH NO2 OH ON NO2 No reaction Et CH OH H20* What is the major product of the above reaction sequence? OME -Et OH...
Predict the major product for the following reaction.
1. excess CH1 NH2 2. Ag20, H20 heat 1. KOH 2. CH3CH2CH2CH,Br 3. H30 d. NH &
Using the reagents list below, propose a synthesis of the
target compound starting from benzene. Enter your answers as a list
of letters corresponding to the selected reagents in order you wish
to use them. You may assume that all reactions are appropriately
worked up and that mixtures of comstitutional isomers can be
separated
Remaining Time: 59 minutes, 08 seconds. Question Completion Status: Moving to another question will save this response. Question 1 Using the reagents listed below, propose a...
give mechanism
3.1 sc)o 2. CH3(CH)&B \ 3. Нзо", heat O/ d) 1. NaOEt 2. dil. H3O OEt 1. LDA, -78°C 2. CH CH2Br f) 1. NaOH, 2 2. H30 1. NaOH, heat g) xs NH3 (SN2) 1. Br2, PBr3 2. H20 h)