Q: 1. CH3M9B. 2. H*, H2O 1. HC(OEt)3 MgBr 2. H*, H20 1. 2.
A: 1. Reaction of lactone with 1 equivalent of grignard reagent followed by hydrolysis gives ketone.…
Q: Br KOC(CH3)/isi b) `OC2H5 1.2 mol CgHsMgBr c) 2. H3O*
A: reactions
Q: NH, CC3 CH;CH,COCI AICI, (i) NH, HNO3 H,SO4 (ii) H CH, Br AICI3 (iii)
A:
Q: HBr, ether с. 1. BH3, THF; 2. H2O2, OH d. CHCI3,KOH е.
A: In organic chemistry reagents helps us to identify the reactions that occur.
Q: CO3)3() + HNO3(aq) Al(NO3)3(a9) H2O) + CO2g)
A: Balancing step by step to given Chemical equation.
Q: SOC2 Br NaCN A [1] (CH3)2CuLi [2] H20 [1] LIAIHA [2] H,0 CH3OH, H* PCC [1] DIBAL-H [1] CH,Li G [2]…
A: The products A, B, D, E, F, G, and H are shown as follows:
Q: 1. NaNH2 2. 1) O3 2) Zn, H30+
A:
Q: MCPE Mg, Et₂C g^ Ź= POCIĄ N HO (!!) PBr3 OH но HOYO 3
A: From alcohols we can prepare different compounds. From alcohol we can prepare alkenes, diols,…
Q: Me NaNO2, HCI then CuBr, HBr Me 'NH2 Ме CH2B. Br Ме NH2 A BrH2C NH2 В Ме Ме Br Ме NH2 C Me Br D
A: Name of compound is 3,5-Dimethyl aniline which is anaromatic amine compound
Q: 4.54 Classify the following redox reactions as combination,decomposition, or displacement:
A: Given reactions, (a) P4 + 10Cl2 → 4PCl5(b) 2NO → N2 + O2(c) Cl2 + 2KI → 2KCl + I2(d) 3HNO2 →…
Q: CH3 1. BH3-THF 2. H2O2, NaOH 1. Hg(0OCCH3)2 THF, H2O CH3 2. NABH4, NaOH
A: Reaction: Mechanism:
Q: O. 1. Br2 SOCII2 KOC(CH3)3 1. ВНз Mg 2. H2О2,ОН Et20 pyr FeBr3 2. HзО*
A:
Q: 1. (CH3)2CHCI, AICI3 2. HNO3, H2SO4 3. KMNO4, NaOH, A 4. H*, H2O
A:
Q: H3CO OCH3 H3CO OCH3 1. PCC 1. H20, H* CH3 CH3 2. CH;MgBr 3. H3o* HN, CH3 он
A:
Q: 1) NaNH2 Ph 2) CH31 3) Na, NH3 Br A
A: In organic chemistry, every reagent has a specific function as per the reactant. Unsaturated…
Q: 1. BH3 2. NaÕH, H2O2 A / 3. TSCI, pyridine 4. NaNg
A:
Q: 1. Pd°Ln, ElN, MECN Me HO 2. NABH4. MeOH 3. CI , EtgN, CH,Cl, Me
A:
Q: aa. 1. Hg(OAc)2, Н-NCH,Ph 2. NaBH4 CH3 bb. HgSO4, H20 H,SO4 c. 1. NaNH2; 2. CH3CH,I 3. Na, NH3
A: Alkenes are the organic compounds which contain one or more double bonds.
Q: 7. CaCl, + K2CO3 CaCO, +OKCI
A:
Q: H* H* COH 1. NaBH4 1. EtMgBr k 2. NH,CI(aq) 2. NH,Cl(aq) H* H2 Pd NH2 I I-Z
A: Major products of Organic reactions
Q: H3PO2 HNO3 Sn, HCI А NaNO2 В CUCN C D H2SO4 HC1
A: Breathing moderate to high amounts of acetone for a short amount of time can irritate your nose,…
Q: Me LOTS Br. 1 equiv. NaN3 DMSO `Br Nal Br acetone Br
A: Sodium alkoxide reacts with alkyltosylate to form ether Primary alkyl halide is more reactive than…
Q: OH + H20 1.CHзMgBr 1. CHзONa CH3OH CH3OH H2SO4 2. Н2о 2. H20 H2SO4 I II III IV V
A:
Q: 1. NaOMe, а. CH3 TsO OTs H3C 2. КОН 3. Hзо", д 1. LDA 2. NBS b. H3C, *CH3 ČH3 с. H*, Br2 H3C, CH3…
A: Here we have write the major product formed in the following reactions.
Q: Identify the major product for each reaction
A: The direct reaction of carboxylic acids with amine results in generation of unreactive carboxylates…
Q: 2a. CH4 + Cl2 -----> HCI + CCI4 2b. SizN4 -----> Si + N2 2c. P4+ Cl2 ----> PCI3
A: According to the Law of conservation of mass " all atoms of different elements must be equal on both…
Q: 1. C3H;MgBr 2. Н,о ? 1. CH;CH,I 2. MeşCO ?
A: Answer, We have Reaction with grignard reagent and methyl iodide.
Q: 1) O3 2) (CH3),S
A: The mechanism is as follows:
Q: H* a H. HO Cl2 b XS CH4 hv 1. NaBH4 2. NH,CI(aq) H2 d Pd
A: Organic Reactions.
Q: Ch, AIC; H,SO4, HgCh `N' KNO3, H2SO4 300°C Br2, fuming H,S04 130°C
A: In Pyridine nitrogen atom is electrons withdrawing group and it's withdraw pi bonded electrons from…
Q: CH3CI A AICI, Sn B• HCI OH- C D NaNO2, HCI, 0°C CUCN E HNO3 -F H2SO4
A: The products are as follows:
Q: 2eq NaNH, 1. 1еq NaNHz II 1. ВН,/THF III 2. НО, На0, На02 H2C=CH2 Br2 IV CH2CI2 2. CH3BR
A: First reaction is addition of Br to alkene. Then elemination
Q: a. CH3 1. NaCN, THF 2. NaSCH3, THF
A:
Q: 1. CH;COCI (c) 2. H2, Pd/C 3. NBS, ROOR
A:
Q: Cl I Br2, Fe AlCl3 J SO3H CH3I, AICI3 K H°OS I2, CuCl, L NO2 Cl
A:
Q: H2SO4 B(OH)3 → B2(SO4)3 +_H2O Sg + SO2 Fe + AGNO3 > Fe(NO3)2 + Ag
A:
Q: А C II NH2 NH, CH,Br H,, Pd Br2 (b) (а) CH3 H
A:
Q: c) 1) Hg(OAc)2, CH3CH;CH2OH 2) NABH4, HO - d) 1) BH3, THF 2) H-Ог, ОН-
A:
Q: OH OH OH SOCI₂, pyr PCI, PBr3
A:
Q: T. NaNHz 2. CH3I 3. H20,H2 SO4
A: In this question we have to tell the product of the reaction.
Q: (CH3),COCH3 HI (CH3),CI CH3I H20 но e OH i) MgBr i) BrMg" ii) HO, HO, ii) H,0
A:
Q: 1 SIO2 Si 2 CaCl2 Са CI MnO2 Mn 4 Feo Fe 5 Fe2O3 Fe 6 H2O2 H 7 Сао Са 8 H2S S CIF3 CI F 10 NH4 H
A:
Q: 1. Name the following molecules. Spelling counts. Br HC CH3 CH3 CI a. -CH3 b. CI-C-CH,CH,CH c. HO H.…
A: The write the IUPAC name of the following molecules.
Q: Nal (1 mol) C3H10CII acetona Br + NaS SNa C4H&S2 b) Br CI + Na,s C4H8S c) Cl
A:
Q: а. NaBHa, CH3ОН b. [1] LIAIH4; [2] H2O с. [1] CН:MgBr; [2] H-0 d. HOCH:CH20Н, Н" е. NaCN, HCI
A:
Q: + Al(NO3)3 a. Al2(SO4)3 + Ba(NO3)2 b. Ca(C2H3O2)2 + K3PO4 BaSO4 Ca3(PO4)2 + KC2H3O2
A: Answer - Balanced equation - Balanced equations are those whose coefficients result in equal numbers…
Q: e) 1) CH2 N2 4. HO cl 2) Ag20 wree tremechaui sm? 3) Hzo
A:
Q: HzO. Br HzO 2) $ CCH2), Mg Br + H2CO H2O 3) $C CH2)s Mg Br + 3 2.
A: “Since you have posted a question with multiple sub-parts, we will solve first three sub-parts for…
Q: CH,CH;OCH;CH, + 2 HBr →: (1) H,SO, NaC=CH H,O*/H,O HOCH,CH,CH,Br (2) CH,=C(CH,); Zn HC1 он CH3 CH2…
A: The products for the given reactions have been mentioned below. They undergo either substitution or…
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- help me please Please fill in the reagents,intermediates, and/or products of the following reactions. all the reactions shall be covered in Chapter 12-15 from Organic Chemistry, 6th Edition by Marc Loudon and Jim Parise.Fill in necessary products reactants or reagants of these reactions. Please note the existence of enantionmers in some cases.Show stereo chemistry and possible outcomes and the steps for the reaction.
- Rearrangements can occur during the dehydration of 1° alcohols even though no 1° carbocation is formed—that is, a 1,2-shift occurs as the C— OH2+ bond is broken, forming a more stable 2° or 3° carbocation, as shown in Equation [1]. Using this information, draw a stepwise mechanism for the reaction shown in Equation [2]. We will see another example of this type of rearrangement in Section 16.5C.Assume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final productComplete the following reactions with the majority products and the missing reaction conditions. Indicate stereochemistry if applicable. Also indicate the type of reaction that took place (SN1, SN2, E1, E2, E1bc)
- 1. What type of reaction is occuring in step 3? (halogenation, hydrohalogenation, reduction, keto–enol tautomerism, dehydrohalogenation, acid-catalyzed hydration, base-catalyzed hydration) 2. Which reagent is necessary for step 3? (Br2, HBr, H2/Pt, NaNH2, H20/H2SO4/HgSO4)Write the structural formula of the organic product for the given reaction between an alkyne and an alkyl halide. The alkyne group is shown and should be entered as "CC" without the triple bond. Enter CC before associated HH atoms (e.g., CH3CH2CH2OCHCHCH3). what is the name of the product. 1.NaNH2 CH3CH2CCH------> product 2. CH3CH2BrI have this task in organic chemistry (book: Brown's introduction to organic chemisty, global edition). Task 10:42. In (a) I have to tell what the funcion of K2CO3 is in step 1. Is it that CO32- take the hydrogen atom in 1-napthol? Will it then be a SN2 mechanism? In (b) I have to name the amine used in step 2 to form Propanolol. But I can't really find out how to come up with an amine that will make that reaction. Here are two pictures of the task:
- Trimethyllead hydride, (CH3)3PbH, can react with methyl bromide (CH3Br) in a homolytic dissociation reaction. What will the lead-containing product be? (CH3)2Pb PbBr2 (CH3)3PbBr Pb metalfor (4) and (5) please provide reactants and why it was chose- For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H2SO4H2SO4, then draw the structures of the minor and major products of the elimination. Picture: Cyclohexane (no double or triple bonds) with a methyl group and an alcohol group (HO 4e- on O) on C1 (bottom) reacting with H2SO4 -> "Major and Minor Products" -The H2SO4H2SO4 is abbreviated as H+H+ in the drawing module. Do not delete any pre‑drawn bonds, charges, or lone pairs. If you accidentally make a mistake, remove the last change by using the undo button on the lower left or revert the drawing palette to the original state by selecting the More menu, then select Reset Drawing. Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation of the carbocation intermediate for the elimination. (Picture 1) -Step 3: This tertiary carbocation intermediate readily undergoes…