ASAP!!  and change 2pentane to 2 -pentanone !! Thanks

Q: 4.) HX is used as a reagent in the reaction below. „NH2 HO. + HX + :NEN: A. What functional-group…

A: The given reaction is Schmidt reaction. The reagent HX used in the above reaction is actually…

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A:

Q: 1. CO2(s) 2. H,0, H2SO4 (3) MgX HO. Grignard reagent Carboxylic acid 1. R,CULI, THF 2. NH,CI, H2O HC…

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Q: 30 Br he 31 + HO. لماذا و( 32 OH 33; phenol e Br 34

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Q: Br 1. NaOCzHg, CzH,он 2. NaOH, H2O 3. Н,о", һeat

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Q: What is the slow, rate-determining step, in the acid-catalyzed dehydration of 2- butanol? Loss of a…

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Q: Draw a structural formula for the major organic product of the rea 0 0 + CH3OH…

A: Products of given reactions are:

Q: Br 1. Mg, ether 2. CO₂ 3. H₂O* omatic alkyl group oxidized into benzoic acid by KMnO4 Ph-R + KMnO4 →…

A: Given are organic reactions. Given reactions involves synthesis of carboxylic acid.

Q: Draw the structure of all organic products formed in the following reaction. NH 1. KOH 2. (CH₂)₂CHCH…

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Q: HO-A-OH HO-C-B-C-OH ethylene glycol (A group) terephthalic acid (B group) The starting materials fer…

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Q: Part III. Structures of Organic Compounds Direction: Draw the condensed structural formula of the…

A: Condensed structural formula is the short hand notation of the atoms of the molecule in a line of…

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

A: Acid chloride is the most reactive followed by  ester and amide is the  stable. Carboxylate ion is…

Q: 5. Which one of the following compounds has the functional group of a carboxylic acid? CH;CO,CH,…

A: Dear student this question is related to functional groups.

Q: CH3- CH2- CH2- Br KMNO, sOCIz A B (c AIBR, H20

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Q: What is the major organic product of the following reaction? (Remember to count carbons!!). HO. ??…

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Q: The reaction of ozone with 2-butene leads to -10 formation of aldehyde + ketone 0 aldehyde + alcohol…

A: Here we have to determine the correct products formed by the ozonolysis of 2-butene .

Q: O || CH3CH2-C-OH (aq) + NaOH (aq) CH3 CH₂-C-0- Na² (aq) + H₂,0 (1)

A: In an acid base reaction, acid reacts with base to form salt and water .This is called…

Q: Which of the following compounds is an ester? CH;C-OH CH CH ĈU

A: Ester is carboxylic acid derivative.

Q: Refer to the following structures: K cont mo NH₂ CH₂-CH-C-OH OI, II, III OI, VI O III, V OI, IV OVI…

A: Esters are compounds with R-CO-R group.

Q: d. KOEt EtOH NaOH, EtOH heat Jam Ph

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Q: B. Draw structures for the products in the following reactions. N. ny NH₂ -N- NH₂ 1. LIAIH4 2. H₂O*…

A: Please find the attachment.

Q: What type of organic molecule is this? нн н-с-с-с H. O-H ketone alcohol O aldehyde organic acid

A: In the given molecule,. -COOH group is present.

Q: Hg (OAc) NaBH Ha S04 3,3-dimethyl-1-butene" 04. THF 4,

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Q: OH CH, H- H,C. CH, CH, H;CO OH -NH

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A: Sodium borohydride is a reducing agent. It converts ketones to secondary alcohol and aldehydes to…

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Q: 9. Which of the following can form a hydrogen bond? A) 2-fluorobutane B) 2-fluoro-2-butene C)…

A: Hydrogen bonding: The hydrogen atom attached to the electronegative atom like fluorine, oxygen, or…

Q: Draw the structural formula of the carboxylic acid formed when each of the following aldehydes is…

A: Oxidation reactions of reactions of aldehydes are pretty common and easy because of their reactive…

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A: The carbonyl compounds aldehydes and ketones are water-soluble but the solubility of aldehydes…

Q: Reaction 2 H3C. H3C `Ph Ph Choose one or more: functional group transformation change in carbon…

A: For each of the given reactions, pick the correct description and the correct reagent.

Q: НО. ОН ҳ Но, ОН ОН ОН NH₂ 0 ОН

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Q: 1. Write out the steps necessary to make trans 2-pentene starting with propyne and any other…

A: The solution is as follows:

Q: CI لمد py .NH OH چه .

A: The reactant in the first equation is acyl chloride and in the second equation is acetic anhydride.

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Q: 10. Identify and name the functional groups in salinosporamide A, an anticancer agent isolate from…

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Q: 10. N‚N-Diethyl-m-toluamide (DEET) is the active ingredient in many insect-repellent preparations.…

A: In this question we are asked to synthesise N,N-Diethyl-m-toluamide from Toluene as shown below-

Q: Organic Chemistry Nomenclature Project Carboxylic Acids CH, CH, CH3 OH pentanoic acid H,C- H;C. H3C-…

A: For the nomenclature  of carboxylic acid we use the following pattern     Prefix + parent chain +…

Q: Which is the major product from the reaction of propene with BH3 followed by NaOH/H202? a)…

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Q: Draw the organic product formed in the following reaction. [1] OsO 4 =CH ₂ [2] NaHSO3, H₂O draw…

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Q: for trans-1.2-dichlorocyo 3. The structure below is Formeterol, a long-acting b-adrenergic agonist…

A: Redraw the structure and label all the functional groups--

Q: H;C. он CH2 Он CH3 CH2 H,C-C- CH3 CH2 он c) CH2 CH2 CH2 но CH2 CH2 b) a) H;C

A: Since you have asked multiparts questions, we will solve the first three sub parts questions for…

Q: OH 1. NaOH, EtOH 2. n-BuBr A nucleophilic substitution reaction is a frequently used method to…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: CH; CH₂ NH₂ + NEN CI N=0 CH, NaNO₂ HCl (aq) NH₂ IV CH, N- ? NH, NÓ,

A: When anilines are treated with sodium nitrite, (NaNO2) in the presence of aqueous solution of…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.