In
other option it is not possible because both are electron widrawing
group. So in forth option only meta position is possible
Question 4 (1 point) Which multistep synthesis is flawless? NH2 Step 1. H2 SO4, HNO3 Step...
Question 40 Not yet answered Marked out of 3.00 Flag question Which sequence of conditions best accomplishes the transformation below? NH2 Select one a. 1) HNO3/H 50. 2) Bry, Ferg, 3) Zn, HCI b. 1) NBS. 2) HNO3/H,50, 3) Zn, HCI c. 1) HNO3/H 504. 2) Zn, HCl. 3) Bra FeBrg d. 1) Bra FeBrg. 2) HNO3/H.S04, 3) Zn. Het uiz/attempt.?attempt=886589&cmid=1097276&page=40 The major product of the reaction below would be: AICI Select one o Question 42 Not yet answered Marked...
Question 1 Not yet answered Marked out of 3.00 P Flag question Which sequence of conditions best accomplishes the transformation shown below? CI Select one: O a. 1) CH3COCI, AlCl3. 2) Cl2, FeCl3. 3) Zn, HCI o b. 1) Cl2, FeCl3. 2) CH3CH2CI, AICI: O c. 1) Cl2, AlCl3. 2) CH3COCI, AICIz. 3) Zn, HCI O d. 1) CH3CH2CI, AICI3. 2) C12, FeCl3
How would you perform the following multistep synthesis ? Benzene to 1,3,5-trimethyl benzene Step 1 HBr, Step 2 Sodium ethoxide, Ethanol, Step 3 Thionyl Chloride, Step 4 KOH Step 1 NaOH, Step 2 Water, Sulfuric acid, Mercury sulfate Step 1 HNO3/H2SO4, Step 2 Sn, HCl followed by NaOH, Step 3 3moles CH3Br, AICI3 b) Step 4 NaNO2, H2SO4, Step 5 Ethanol Step 1 3moles CH3B, AIC13, Step2 HNO3/H2SO4, Step 3 NVH2, Step 4 NaNO2, H2SO4, Step 5 Ethanol, 3Moles CH3Br,...
What are the best reagents for the following transformation? o NH2 NH O2N O H2SO/HNO3 01. CH3COCI, AICI: 2. H2SO4, HNO3 3. Zn(Hg), HCI O 1. CH3COCI 2. H2SO4, HNO3 O 1. H2SO4, HNO3 2. CH3COCI, AICI:
* Which of the proposed reaction sequence is best to carry out each of the following conversion? Assume ortho and para isomers can be separated. CO2H 0-0 NH2 a. 1. CH3C1, AIC13 2. HNO3, H2SO4 3. KMnO4, H30+ 4. Hz/Ni 1. CH3C1, A1C13 2. KMnO4, H30 3. HNO3, H2SO4 4. H2/Ni 1. HNO3, H2SO4 2. H2Ni 3. CH3C1, A1C13 4. KMnO4, H30 1. HNO3, H2SO4 2. CH3C1, A1C13 3. Hz/Ni 4. KMnO4, H30
3) Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction with 1,3-butadiene? A) CH2CHOCH3 B) CH2CHCHO C) CH3CHCHCH3 D) (CH3)2CCH2 E) CH2CH2 5) Which of the following fails to form benzoic acid when heated with chromic acid? A) 1-phenylethanol B) 2-phenylethanol C) 2-phenylheptane D) 2-methyl-2-phenylheptane E) 1-phenylheptanol 11) How can the following synthesis be carried out? A) HCOOH; HNO3/H2SO4 B) CH3Cl/AlCl3; HNO3/H2SO4; H2CrO4, heat C) CH3Cl/AlCl3; H2CrO4, heat; HNO3/H2SO4 D) HNO3/H2SO4; CH3Cl/AlCl3; H2CrO4, heat E)...
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Testbank, Question 046 Provide the reagent(s) necessary to carry out the following conversion. NO2 NH2 H2 and Ni 2. H20 Fe and HCI Zn and HCI O all of these Testbank, Question 057 Predict the product for the following reaction. 1. CH3CH2Br 1. CH3Br NH2 2. -NH4Br 2. -NH4Br Testbank, Question 070 Predict the product for the following reaction NH2 H2SO4 HO NH HN IV C II c IV
Testbank, Question 046 Provide...
QUESTION 1 predict the major product HNO3 'ocH3 H₂SO4 a) cocta NO2 octz b C QUESTION 2 The following compound has four aromatic rings. Rank them in terms of increasing reactivity toward electrophilic aromatic substitution. (least to most reactive) -N B С A<B<C<D B<C<DCA B<D<C<A A<<< QUESTION 3 Identify reagents to prepare the following compound OM Lockta NO2 NO2 + Aldz b) 'octz اه Aldo + D) + OCH₃ c) either a or b( both work) а b с QUESTION...
Answer A-C
3. Predict the product of the sequence of reactions shown: 1. Fuming Sulfuric acid a. 2. Cl2, FeCl3 3. H2SO4 Br 1. CH CVAICls b. 2. HNO3/H2SO4 3. Zn/HCI 4 NaOH tAICI, 1. AlCl3 cl c. 2. Zn (Hg), HCl, heat
Which of following is the best starting material for the reaction below? 1. (CH3)2NH ? 2. LIAIHA 3. H20 'N NK CN NH2 What is the major product in the following reaction? 1. DIBAL 2. H20 O H O OH OH СІ Which reaction sequence would accomplish this transformation? CN H2SO4/HNO3 Br2 NaNO2/HCI CuCN O Br2/FeBr3 H2SO4/HNO3 KF NaNO2/HCI O H2SO4/HNO3 Zn(Hg)/HCI NaNO2/HCI CuCN o H2SO4/HNO3 Zn(Hg/HCI NaNO2/HCI HBF4