Q: Br2 CH2 H20
A: ->first of all there is formation of cyclo bromonium ion which can be broken by H2O.
Q: Save Share II as starting mükerials show & synthusis that gets this produet benzene Cyelohexáura NO2
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A: Given reactant is : 3-methyl-3-pentanol.
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A: Reaction 1 : Br2 addition to alkenes produces trans -1,2-dibromo compound. Reaction 2 : HBr addition…
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Q: The reaction below is considered one: * Image without caption Oxidation Reduction Replacement…
A: in the given reaction, the H2 is added to the alkyne. this reaction is called birch reduction.
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Q: TRUE OR FALSE: Allylic carbons can be a substrate for halogenation via electrophilic addition.
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Q: A Moving to another question will save this response. Question 5 Which one of the following…
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A: Addition of H2O to alkyne:
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Q: ? Br
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Q: Circle the electrophilic and nucleophilic atoms in each substitution reaction below. Provide the…
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Q: 1. Write in the product: 1. O3 1-isopropyl-4-methylcyclohexene 2. Zn, H30*
A: O3 break the double bond and oxidise it.presence of zn metal is stop the further oxidation
Q: OH
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Q: ОН НІ, Н,О CH;CHCH3 ICH2CH3 + heat
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Q: 1. Which alkene is the major product of this dehydration?
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Q: a. Label the reactive features, highlight the most reactive one, then highlight what it needs. Also,…
A: Hydroboration reaction
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Q: True or False for the product of this reaction. HOOCCH CH>COOH + Heat --> Cyclic dicarboxylic acid
A: The reaction taking place will be as shown below.
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A: LiAlH4 is a reducing agent which reduces acid to alcohol.
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Q: octane from 1-butene
A: The structure of 1-butene is shown below. The structure of octane is shown below.
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Q: QUESTION Complete the following synthetic transformation by selecung from the list of reagents below…
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Q: (d) Complete the following reaction: hv (i) Cp2TiMe2 +2 [RCH=CHR] AlMez (ii) [Cp*Ir"Cl}]2 (iii)…
A: NiCl2(PMe3)2 + RMgCl → ?
Q: Questions 1 and 2 Solvents used are hexane,toluene,acetone,ethanol, and water
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A: Retro synthesis is the conversion of the target compound to its precursor or simpler structures.
Q: G. Basic Oxidation Test Sample Нехane Нeptane Cyclohexane Cyclohexene Benzene Toluene
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Please do the following question step by step
A. butyne + Br2 in CH3OH
B. 1-butyne + disiamylborane followed by H2O2, -OH and H2O
Step by step
Solved in 3 steps with 2 images
- How many moles of Bra are required to completely halogenate the alkene?A. One moleB. Two molesC. Three molesD. Four moles What is the expected arrangement of the bromine atoms relative to each other amongthe carbon involved in pi bonding?A. anti-conformationB. syn-conformationC. trans-configurationD. cis-configuration What happens to bromine when it is adjacent to an alkene during a chemical reaction?A. Bromine becomes stable. (? kasi before brown siya/acidic tas naging colorless? Jk ewan)B. Bromine becomes polarized.C. Bromine becomes hybridized.D. Bromine becomes acidic. The relative arrangement of bromine atoms in the product is primarily due to:A. ElectronegativityB. RepulsionC. Hydrogen bondingD. Atomic weightWhat is your observation after the reaction?A. A yellow flame is produced.B. Bromine water decolorizes.C. The alkene becomes denser.D. A brown precipitate forms.os 1) NBS 2) NaOEt/EtOH 3) BH3 4) H₂O₂/NaOH/H₂O 5) NaH 6) CH3CH₂OTs *In the problem above, Step 1 replaces the H atom behind the wedged methyl group with a Bratom.[Review Topics] [References] Br H3C CH3 H3C H3C 1. Aqueous ethanol + HO +] H. CH3 H. CH3 BH3 O-BH3 f=Sn1 Nucleophilic substitution g = Sn2 Nucleophilic substitution a = Proton transfer d = El Elimination b Lewis acid/base e = E2 Elimination c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - gf answers. 2.
- What is the major product when 2-iodopentane is used in dehydrohalogenation reaction. A. 2-iodo-1-pentene B. 2-pentene C. (E)-2-pentene D. (Z)-2-pentene E. (Cis)-2-penteneChoose the major product when 2-bromo-2-methylpentane is treated with sodium ethoxide in ethanol a.(E)-4-methylpent-2-ene b.2-methylpent-2-ene c.(Z)-4-methylpent-2-ene d.2-methylpent-1-enePlease do the following question step by step . A. 1,3- cyclopentadiene + CH2 = CH – COOH B. 2-methyl-1,3-pentadiene + trans – CH3- CH = CH - COOH
- H3C OH OH CH3 1,3-pentanediol + B OMe OME OME MeO... CH3 H3C OMe benzaldehyde dimethylacetal catalytic Me 0:0 OH FO (p-TsOH) CH3CN H... MeO, OMe OMe e a & H3C CH3 H3C CH3 H3C CH3 C D A HO E HO OCH3for this question. Draw a structural formula for the missing product in the following reaction. 0. NaHCO3 H20 ? + CO2 + H20 + CH3C-OH • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. C P. opy aste [F **** C - Visited CH4 ChemDoodle Retry Entire Group 5 more group attempts remaining Submit AnswerPlease draw out all missing parts of the reaction like as in reagents, products starting materials) H3C CH3 H30", A H,CH,Co OCH,CH;
- I. Name the following benzene derivatives in accordance to General Nomenclatures and IUPAC rules. NO2 NO2 CaHs Co ty 1. 4. CH-CH2 CH-CH NO cOcty CH2 NO2 NOz 5. NO cOcto I 3. 6. NH, 2. NO2 Authored by: Sensei Wilmark Palacios 7. 8. NH, cooH OH CAg 9. 10. COH I 2.Bn Draw the structure of the major organic product formed from the reaction below. Bn H ད ་ + HỌỌC. NH2 N DCC .... NH H BnDraw the structure for each compound.a. (R)-3-methylhexaneb. (4R,5S)-4,5-diethyloctanec. (3R,5S,6R)-5-ethyl-3,6-dimethylnonaned. (3S,6S)-6-isopropyl-3-methyldecane