(a)

Step 1: Bromination of benzene via electrophilic aromatic substitution.
Step 2: Production of Grignard reagent.
Step 3: Formation of secondary alcohol from the reaction of Grignard reagent with benzaldehyde.
Step 4: Oxidation of secondary alcohol to ketone.
(b)

Step 1: Formation of Grignard and then reaction of Grignard reagent with CO2 followed by acidic work up gives carboxylic acid.
Step 2: Formation of acid to acid chloride. Then acid chloride reacts with ammonia to form amide.
Step 3: Dehydration of amide with phosphorous pentoxide gives the nitrile.
(c)

Step 1: Aldol reaction gives the aldol product.
Step 2: Dehydration of aldol product to give the conjugated aldehyde.
Step 3: Reduction of aldehyde to alcohol.
(d)

Step 1: Oxidation of toluene to benzoic acid.
Step 2: Conversion of acid to acid chloride.
Step 3: Reduction of acid chloride to aldehyde.
calculuate valence electrons for each complex
(a) [Mn(H20)]3+ (d) [Fe(H20).]3+ (b) [Cr(H2O)6]2+ (e) [Co(NH3)4] * (h) [Pd(NH3).]4+ (c) [V(H2O).]2+ (1) [Ni(H2O)]2+ (1) [Re(CN).]3- (g) MoF6
Practice Set-lll SET-II 1) C.HNH 1. 2) LIAIH, in ether ? 3) H2O) 1) NaOC Hs ; then CeHsCH CH-Br 2. HCO2C2H5 2) H20 ? & heat H CO2C2H5 3) SOcl, ; then AICI3 & heat 1) Mg in ether 3. ? CHa-CI 2) (CH) CH-CN H2C 3) H3O CH3 1) NaOC,Hs; then CHs-I 2) H3O& heat 4. ? O-CaHs )CHCHO & NaOH; heat SET-III Stage Two Stage Three Stage One
Practice Set-lll SET-II 1) C.HNH 1. 2) LIAIH, in...
Solutions of coordination compounds [Co(H20)2(NH3)3Br]CI and [CoCl(H20)2(NH3)3]Br are placed in two separate test tubes and labelled A and B, respectively. Drops of lead nitrate solution are then added to each test tube. In which test tube do you expect a precipitate of lead chloride to form (Answer with A or B only)? What type of isomers are A and B? [VERY IMPORTANT: Type your answer as follows: letter of choice; name used to describe the isomers (DO NOT write the...
СО,Н сО-СН-СH, a. СО-Н "CО,Н Н,СО BI H3CO Cl b. H3CO Н,СО ОСН) ОСН, СО,Н Ph "СО-Н -Br Н,СО- Br d H3CO Н,СО OCH3 ОСН; NH2 Н,СО. H2CO Br e. Н,СО H3CO ОСH, OCH3 mescaline found in peyote (also provide the IUPAC name) .CH3 NH2 f. H3CO НО CN g.
СО,Н сО-СН-СH, a. СО-Н "CО,Н Н,СО BI H3CO Cl b. H3CO Н,СО ОСН) ОСН, СО,Н Ph "СО-Н -Br Н,СО- Br d H3CO Н,СО OCH3 ОСН; NH2 Н,СО. H2CO Br e....
NH4+(aq) + H2O (l) BLUE <--GREEN--> NH3(aq) + H3O+(aq) YELLOW NH4+ + H2O= Blue. NH3 + H3O = Yellow. Mix is green at equilibrium. Q: When adding sodium hydroxide solution, the color of the equilibrium mixture changed from green ---> yellow. a. In which direction did the equilibrium shift? (L) left or (R) right b. Explain answer to a. Which ion was added or removed from the equilibrium mixture?
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
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
3. The reaction of the anti-cancer drug cisplatin with water is Pt(NH3):C12(aq) + H20(I) → Pt(NH3)2(H2O)Clı"(aq) + Cll(aq) The rate of this reaction increases by a factor of 15 when the temperature is increased from 25°C to 50°C. What is the activation energy for the reaction?
Name the following compounds: 5. a) CuCla]2 b) Cr(H20)(NH3)]2 c) [Cr(H2O)4(NH)] SO4 d) K3[Fe(CN)6]
1. Predict the products of the following reactions. excess NaNH2 THE Br Br H 1. NaNH2 2. CH3CH,Br H2SO4, H20 Hz, Pd/BaSO4 quinoline, CH3OH Na, NH3 1 equivalent HBO NaNH2 Br (excess) 1. Sia,BH, THE 2. H2O2, NaOH HgSO4 H2SO4 H2O