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A:
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A: SN2 mechanism:- It is a nucleophilic(N) substitution(S) bimolecular(2) reaction. This SN2…
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A: This is a sequencial reaction in which P convert into Q by heating with KOH and Q into R by acid…
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A: If heated once the product is below.
Q: Does the compound below undergo saponification reaction? Why? C-OCHCH, 一 CH,
A: Saponification reaction is defied as the reaction of ester in presence of acid or base which will…
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A: Olefin metathesis is done in the presence of Grubbs Catalyst as shown below.
Q: nach
A: Given reaction is Sn2 substitution reaction. Hence we get product with inverted stereochemistry.
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Q: Considering the molecule D-Galactose below, HO- H HO- a. b. H CHO OH H -H -OH CH₂OH Which galactose…
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Q: What reaction conditions are needed to convert (R)-2-ethyl-2-methyloxirane to (S)-2-…
A:
Q: (ii) Show the pathway for the synthesis of a-methylbutyric acid from ethanol.
A: Interpretation - To show the pathway for the synthesis of α-methyl butyric acid from ethanol -…
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Q: c. 2,3-dimethylhexan-3-ol is heated in the presence of sulfuric acid
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A: Given:
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A: The organic products formed in attached reaction can be drawn as,
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A: Structure
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Q: 2-methylpropene 4-methylpentanal
A:
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Q: From these, what is the structure of azodye produced? но OH -NH2 H3C Но
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A:
Q: Which of the following will be the dominant product of the dehydration reaction shown? H3PO4 H20, A…
A:
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A: LiAlH4 reduces carboxylic acid so as to form corresponding alcohol.
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A: For finding the congugation, let us try to draw its resonating structures.
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A: How would the reactant react with (CH2=CH)2CuLi ?
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A: The reactions taking place are,
Q: Which of the following method is the best method for the synthesis of hexanal A.) Method:…
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A: Option a is correct .
Q: the structure of (R)-1-cyclopropylprop-2-yl propionate
A: The structure of the given compound can be drawn as
Does the compound below undergo saponification reaction? Why?
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- Draw a structural formula for 2-methylbutanoic acid. O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. 8 CH4 #[ ] در ? ChemDoodle4. Draw structural formulas for all possible monohalogenation products that might be formed in the following reactions, then assign them IUPAC names. (a) + Cl₂ lightIn an advanced synthetic chemistry experiment, a researcher prepares a compound, ZY-7, by reacting a ketone (C5H10O) with hydroxylamine (NH2OH), followed by heating in the presence of an acid catalyst. The resulting compound, ZY-7, is then treated with a solution of sodium nitrite (NaNO2) and hydrochloric acid (HCl) at low temperature. Identify the class of compound that ZY-7 most likely belongs to after this series of reactions." A) Amide B) Oxime C) Nitro compound D) Diazonium salt E) Ester Don't use chatgpt please provide valuable answer
- Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH,—O—C—(CH2)—CH=CH-CH,—CH=CH—(CH2) — CH3 CH-0- -(CH2)–CH=CH(CH2)CH3 O CH,—O-C=(CH2)=CH=CH(CH2)—CH3 Separate each name with a comma and a space. You will find useful information in the ALEKS Data resource. type your answer...7) You want to synthesize 3-methyl-2-pentene from 2-chloro-3-methylpentane. Which reagent would you use? a. HCI, heat b. NH:(aq), 25°C c. CH:CO2NA, CH:CO2H, heat d. CH3CH2ONA, CH3CH2OH, heat e. CН:CH2ОН, heat4.) HX is used as a reagent in the reaction below. „NH2 он + HX + :NEN: + A. What functional-group transformation occurs in this reaction?
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