`NH2 II OCH3 ONa II IV

Q: What is the rate-determining step in the mechanism of an electrophilic substitution reaction of…

A: The aromatic electrophilic substitution reactions take place in two steps. The first step is the…

Q: Instructions: Give an acceptable name for eachester. CHỊCH, COCH, A. B. CO,CHỊCH, C.…

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Q: Q4. The herbicide oxyfluorfen can be prepared by the reaction between phenol and an aryl fluoride.…

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Q: What is an acceptable or preferred IUPAC name for the following compound? a.…

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Q: 4. Draw the proper products for the following acid/base reaction. OMY

A: Base is species which abstracts proton and acid is species which donates proton. As we know alpha…

Q: MCQ 16: In SN2 mechanism 'S' stands for A. subordinate B. substitution C. sub-reaction D. systemic…

A: Answer B) substitution

Q: Place reagent combinations in the out to successfully carry the following transformation. ? Ph Ph…

A: Lithium aluminium hydride is strong reducing agent...it reduces azide into primary amine..... R-N3…

Q: Rank the following carboxylic acid derivatives in decreasing order (most to least) of reactivity…

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Q: How is the nitrogen of the oxazole similar or different to the two nitrogen’s that are found in the…

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Q: Which of the following is the correct order of decreasing leaving group ability in nucleophilic acyl…

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Q: Why is pyridine a basic compound while pyrrole is not?

A: Pyrrole and pyridine are heterocyclic aromatic compounds. The basicity of these compounds can be…

Q: 5. a. Clearly identify the most acidic H atom in each of the structures shown below. Circle or draw…

A: The acidic hydrogen is the hydrogen atom which will easily released from the compound and make the…

Q: The bicyclic ketone shown below is first treaterd with a base, then ethyliodide is added to form the…

A: We have given the different bases conditions but the best suitable condition for  transformation is…

Q: Which of the following compounds is not named correctly? O a. 2-Methyl-3-heptanone -…

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Q: CH3 H3C

A: As we know, electron withdrawing groups decreases the ring towards electrophilic aromatic…

Q: Give broad explanation about ferric chloride test.

A: A question based on qualitative analysis, which is to be accomplished.

Q: Which member of each pair is a better nucleophile in methanol?

A: “Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: 1. By what type of mechanism does the following aromatic substitution reaction proceed? Draw the…

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Q: Which of the following alkyl halides would afford the indicated product upon reaction with sodium…

A: The given alkyl-halide undergoes E2 reaction with the…

Q: What explains why many aldehydes and ketones can undergo self- condensation reactions in basic…

A: we have to select the correct statement for self- condensation reaction of aldehyde and ketones

Q: 3Jab = 10 Hz На Hb 3Jbc = 7 Hz CI CI Hc Hc

A: Jab = 10Hz Jbc=7Hz Ha will split Hb into doublet of 10Hz separation, Later Hc will cause that…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. Hg(OAc)2, H₂O 2. NaBH4,…

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Q: Rank the following groups in order of basicity, nucleophilicity, and leaving group ability. a. Rank…

A: A)We know the basicity of a group depends on the ability to donate a lone pair of electrons to form…

Q: — -17 Give the IUPAC name for the following compound: Br CO₂H A. 3-bromo-5-methylheptanoic acid B.…

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Q: . Reaction with Tollen’s reagent 2. Reaction with Fehling’s reagent 3. Reaction with dilute NaOH

A: Tollen's solution is used to differentiate between aldehyde and ketone. It is a solution of silver…

Q: TEST SAMPLE FORMULA OBSERVATION III. Electrophilic aromatic substitution Acetanilide Naphthalene

A: This is the concept of Electrophilic substitution reaction.

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.