What is the BEST way to carry out the following transformation? H. KMNO4/H3O+ ВНз; NaOH/H202 O H2/Lindlar; O3; Zn/H3O*

Q: draw all four products of this reaction. Assume that the reaction is acidified to pH 2 after…

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Q: For each pair below, predict which is the most favourable to undergo an E2 reaction. Explain your…

A: 1- At heating condition, E1 reaction is most favourable because first formation of carbonation then…

Q: 19. Give mechanistic explanation for the following transformations. SPh SPh Dess-Martin HO TEMPO (1…

A: 19. Given reactions,

Q: HC=CH The synthesis above can be performed with some combination of the reagents listed below. Give…

A: For deprotonation of acetylene we need strong base such as NaNH2.

Q: Which substance should we take to carry out the following transformation Fe* Select one: a. H2O2 Ob.…

A: Oxidation is defined as the process in which there is increase in the oxidation state while in…

Q: Which pathway will this reaction likely take? NaSH ? SN1 O SN2 O E1 E2

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Q: Arrange the following compounds in their ease of undergoing an SN2 reaction: a. CH3CH2CH2-Cl b.…

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Q: Give the major product for the reaction below. A H20 HCI cold, dilute B KMNO4 KMNO4, OH, heat E HBr…

A: The reactions are summarized as: The acidic hydration of alkenes takes place according to…

Q: Which of the following is the best method to carry out the following transformation? O 1. BH3 2.…

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Q: Which synthesis plan is best to bring about the following transformation? но ? O 1. H2SO4 2. heat…

A: There occur overall elimination reaction but most substituted alkene does not formed .it means there…

Q: H3C. CH3 ? H3C. CH3 но снз 27. The reaction shown above may be best carried out by reacting…

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Q: Predict the outcome of the following solvolysis reaction in Ethanol from the products shown: CH3 il…

A: Solvolysis follows SN1 mechanism. Retention of product takes place.

Q: Write the products of tollowing reaction sequence CH3 ス. NaCN H20 NaOH Br2 light OH Hz CrzOz Zn HzO…

A: Note: According to our guidelines we are supposed to answer only first three subparts. Kindly repost…

Q: Which solvents favor Sy1 reactions and which favor SN2 reactions? a. CH,CH,OH b. CH,CN c. CH,COOH d.…

A: Protic solvent favors SN1 reactions while aprotic solvent favor SN2 reaction. (a) CH3CH2OH: it is a…

Q: Choose the best reagent from the list below for carrying out each transformation. Place the letter…

A: In this question, we will select the best reagent for the given transformation. You can see the…

Q: 57. Which structure is expected to emerge as the product of the reaction between the given alkyl…

A: For an E2 elimination the stereo electronic requirement is the leaving group and the -H atom must be…

Q: Propose a reasonable synthetic route for the following reaction: CH, CH; HNO3 (B) ? HNO, (А)? (C) ?…

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Q: Which of the following is the best method to carry out the following transformation? - OH (a) H₂SO4,…

A: We will draw all the product of each reaction.

Q: please give correct answer.

A: H2SO4, heat can't be used because it's will removed NH3 from amide and give carboxylic acid not…

Q: Which compound would be the product of the reaction sequence shown below? MgBr 2. H30*/H20 3. РСС 4.…

A: RMgBr is a grignard reagent and it attacks the carbon attached to double bonded Oxygen atom and join…

Q: 4. Give the products of the following reactions. CH₂ (i) KMnO₂. OH, A a.) (ii) H₂O* b.) CH3COOH +…

A: Given reactions are : Give the products of the following reactions = ?

Q: Which of the following statements about nucleophilic reactions are generally true ? SN2 reactions…

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Q: Provide the reagents necessary to carry out the following conversion. O H2, Pt Brz, CCI4…

A: The given conversion is an oxidation reaction which is carried out such that double bond remains…

Q: Carbocation Rearrangement in the SN1 Reaction of 2° and 3° alcohols with HX ?

A: Nucleophilic substitution reactions follow two types of mechanism, i.e., SN1 and SN2. SN1 mechanism…

Q: 1) NaOH HO, 2) CHCH 1) NaOEt B 2) CHы 1) NaOEt 1) NaOH OEt 2) CH,CH,Br 2) HO", heat NaOEt OEL 1)…

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Q: Which synthetic strategy would efficiently bring about the following transformation? ? HO OH O 1.…

A: We have to synthesize  1-phenylethane-1,2-diol from  1-chloro-2-phenylethane using suitable…

Q: If the -CH3 group is an activator and an ortho-, para- director (directs the position of the…

A: -CH3 group is an electron-donating group because of the + I effect .

Q: Choose the best reagent from the list below for carrying out each transformation. Place the letter…

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Q: -CH3 H3C. CH3 Piquindone ) Complete the blank boxes by filling in the missing structures. ii) Write…

A: Organic reaction.

Q: > Br O It depends on the solvent O SN1 O SN² O E1 is synthesized in H₂0 at 50 °C to produce E2 OH…

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Q: Which reagents will give the transformation shown? LOH (1) Вн3: (2) Н2О2 a. (1) Hg(OAc)2; (2) NaBH4…

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Q: Complete the starburst scheme below by predicting the product of each reaction. CH2N2 HBr 03,…

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Q: Br NaCN H30* A 1. LIAH4 2. H20 C |(CH3CO)20 I

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Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H20 + МеОн HO, OMe cat.…

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Q: How would you carry out the following conversions? More than one step is needed in each case. b.

A: The reactions given are,

Q: Predict the product of the reaction shown here. 1. BH3 THF (excess) ? 2. NaOH, H2O2, Н,О…

A: Addition of BH3 on double bond of alkene takes place according to anti-markovnikov rule. In this…

Q: Which synthetic strategy would efficiently bring about the following transformation? ? HO- OMe OMe…

A: The following conversion take place in presence of Hg(OAc)2,H2O / NaBH4.It is oxymercuration…

Q: Which of the following reaction scheme leads to the synthesis of 4,4-Dimethylhex-2-yne? ... 1)…

A: Option A will be correct.

Q: Which Sn2 reaction would be expected to occur most slowly? O A. CH3CH2B + CN1-i B. CH3CH21 + CN1-i…

A: More good leaving groups more will be the reactivity of alkyl halide in SN2 since order of leaving…

Q: 1. H2SO4, heat 2. НCСІ, H-02 LOH d.

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Q: The transformation above can be performed with some reagent or combination of the reagents listed…

A: The above given transformation (convention) of one molecule into another molecule can be carried out…

Q: Acetoor

A: Nucleophilic Substitution Reaction: In the nucleophilic substitution reaction, one nucleophile…

Q: What set of reagents can best accomplish the following transformation? A) PCC in CH2C2 B) AICI3 C)…

A: We have to tell reagent used to bring the above transformation.

Q: What reagent(s) is/are appropriate for the fifth (and final) step of the synthesis, shown below?…

A: In this reaction , a secondary alcohol is converted to ketone. This is oxidation process . So…

Q: What is the predicted major product of the reaction shown? H3O* Br2 + H3O* Br Br + H3O* Br + H3O* IV…

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Q: (10) Please find out the most reactive substrate in Sn2 nucleophilic substitution. А. CH3 Br В. С.…

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Q: Propose a reasonable synthetic route for the following reaction: II CH,CH,-C-CI Zn(Hg) (1)? (2)?…

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Q: noose the best reagent(s) for carrying out the conversion of the reaction below CH3CH-CHCH2COOH -->…

A: For the given reaction, oxidation of alkene occurs.

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.