30. Provided a detailed mechanism showing all intermediates and the proper curved-arrows shown how chemical reaction below takes place. OH H,SO,(aq) + H,0 Heat

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

A:

Q: H-Br

A: The reaction taking place is given as,

Q: a) Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium azide…

A: Reaction mechanism of chlorocyclopentane with sodium azide is drawn as,

Q: О О ОН 1. NaBH4, MeOH 2. H2O

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1 eq. H2O HO, MEOH OMe cat. H-A…

A:

Q: Propose a plausible mechanism for the following reaction: (H,SOJ

A: Interpretation -  To tell about the possible reaction mechanism for the following given reaction…

Q: 23. Which reaction or statement regarding nucleophilic substitutions is incorrect? A) XCI + 2 H₂O…

A:

Q: Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution,…

A: This reaction is diazotization followed by substitution some rearrangement and elimination reaction…

Q: (d) Propose a reaction mechanism to account for the following reaction. AICI3

A: In this question we have to tell the mechanism of the given reaction.

Q: cess CHCH-C 1 KMKO, NaOH HO AICI, H$O. 2. H0

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Q: Osaw the Yeaction mechanisms for the reduction NABHU g benzshenone using Reduction (o.138g) NABH4…

A:

Q: 3) Write a detailed mechanism of: CH, CH. HNO" H'SO O,N

A:

Q: Provide the product and mechanism for the reaction: ОН CrO3, H,SO, H,0

A: This reaction is an example of Jone oxidation. Mechanism of Reaction:

Q: Provide a detailed step-by-step mechanisms for the reaction shown. CH;CH2SH + Br, + NaOH

A:

Q: D. Provide reasonable mechanisms for the following reaction H NaOH, H₂O, A

A: Aldol condensation: The alpha hydrogen of carbonyl compounds is acidic in nature and it is removed…

Q: 4. Show the detailed mechanism for the following reactions. Label steps (Sn2, protonation..), and…

A: We have given the organic reaction and we have to find the mechanism of the reaction.

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: Provide a plausible arrow pushing mechanism for the reaction below. OH LOME TSOH, H20 OMe

A:

Q: Propose a mechanism for the reaction shown below

A: Please find below the reaction mechanism.

Q: CI BiCl3 (5 mol%) CI D, 24 hrs.., neat CI

A: The objective of the question is to write the detailed mechanism of the given transformation. In…

Q: 18. Show the mechanism arrows and product for the rate determining step of the Wolff-Kishner…

A: The mechanism arrows and product for the rate determining step of the Wolf-Kishner reduction has to…

Q: 3) write a detailed mechanism of: OH он CHIČCI AICL3

A: The above reaction is an example of friedal-craft acylation reaction . It is a type of electrophilic…

Q: H2NNH2, KOH Hао, heat

A:

Q: aq Br2

A:

Q: (a) PHOOC-CH,-C-CH,-COOP. (1) KCN, A (2) H,0® (o) СООН Onl

A:

Q: но H2SO4,Heat

A:

Q: Show the detailed mechanism for the following reactions. a. он b. H H OCH3 CH;OH H

A:

Q: Propose a detailed mechanism for the reaction below. لعلام , AICI3

A:

Q: H OH + H-CI = `CH, CH,

A:

Q: NEN N. +] の☆

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. You may abbreviate the…

A: This is an example of Diels-Alder reaction followed by cyclization and aromatization.

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

A:

Q: Select the final product from the following reaction sequence: 1. HNO3, H„SO4 2. H2, Ni 3. HNO,, HCI…

A: Benzene undergo nitration in first step and in subsequent steps diazonium salt is formed.

Q: Predict the product 1. KOtBu A Me Bri Ph. 2. Cl₂, MeOH Me Please let me know the detailed process…

A:

Q: the following reaction go through an SNl or Sn2 mechanism, both, or not proceed as written? Explain…

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Q: :0: || CH3-C-CI: :0: || CH,-C-S-CH, H CH3-SH + + |

A:

Q: NH2 H* (cat.) но. HO, H* (cat.) 1) PPH3 2) nBuLI Br H.

A:

Q: 2а. with ammonia. Provide a detailed, stepwise mechanism for the reaction of propanoyl chloride 2b.…

A: Answer:- This question is answered by using the simple concept of chemical reaction of organic…

Q: 5) Provide the products necessary to complete the synthesis below. Indicate what mechanism was used…

A: The above organic transformation is given below

Q: .CI .CI aq. HBr 65 °C HO. Br

A: The reaction taking place is given as,

Q: NGOH/H,O 4

A: Since you have asked multiple question, we will solve the first question for you as per our…

Q: 5. Using curved arrows, showing key intermediates and any formal charges, propose a detailed…

A: Epoxide ring opening can take place in either side of ring which depends on the condition of the…

Q: HN KON HC Her. H0

A: The mechanism of the following is:

Q: Provide the major organic product of the reactions shown below. Show the from each step shown below.…

A: ->Na2Cr2O7 is oxidizing agent which can oxidize primary alcohol to carboxylic acid.…

Q: The following reaction schemes have flaws as presented. Which of the following statement is the best…

A: Given scheme is an example of electrophilic substitution reaction. In this reaction, Friedel craft…

Q: 30 Cl2 H20

A: Since the alkyne group is electron rich. Hence it will attack on Cl2 and form a intermediate with…

Q: 3. Show a plausible mechanism for the reaction below. , CH NH2 EIOH, cat. HCI H,C- -CH, CH "NH2

A: The plausible mechanism for a given reaction has to be drawn.

Q: Propose a plausible mechanism for the followng reaction INa, NH3 (liq) 2 NH CI

A: Reduction is the reaction of addition of 2H atom across carbon-carbon double bond or triple bond…

Q: 3) Write a detailed mechanism of: CH. CH HNOT HYSO! "NO.

A: Given is the reaction between Toluene in presence of nitric acid and sulfuric acid.

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.