3. Reactions H3C OH [0] CH3 H3C OH H2 CH CH [0] H2C CH3 H2ċ-CH2 CH3 CH H2SO4 HOʻ H2C CH H,C-CH2 of

Q: Determine the product of the reaction: CH,—сн—CH,—он + н ČH, a) CH,-CH-CH, Cl b) CH3-CH-CH3 CH3 c)…

A: In the given reaction, the reacting species is 2-methyl-1-propanol. It is primary alcohol that…

Q: H. D- -Br a) NaCEN H- -H- CH2CH3 I DMSO H. D- H- NaCEN Br- H- b) CH,CH3 DMSO

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Q: Determine the product of the ff. rxn steps 1. CH;NO,/OH- 2. Sn/HCI 3. ΗΝΟ A. В. C. D. OH -NO2 NH2 OH…

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Q: :C: H :CI: :CI: H. CH3 C=C H -CI: H3C-C-C-CH H3C CH3 CH3 Add curved arrows for the first step. Draw…

A: The curve arrow is given below

Q: Reagents Available a. CH2=CHCH,CI, AICI3 b. CН-Br2, ОН c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI,…

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Q: bel each structure as Z, E, or neither. H₂C CH3 (b) H H CH3 CH3 (c) Ph H₂C CH₂CH3 CH; (d) H₂C H CHO…

A: Label the structure Z,E or neither:

Q: using the IUPAC rules name every (all four) molecule.

A: The given structure is, From the structure it is clear that, The longest carbon chain has 7 carbon…

Q: i) CH,MgBr Cycloheptanone A (C3H160) B (C3H14) i) H20 Heat Ozonolysis HO он PUH2 C (C3H1402) E…

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Q: (X) > (excess) Benzene forms a monosubstituted product with (X) irrespective of it's quantity. So(X)…

A: Electrophilic substitution of benzene is the one where electrophile substitute the hydrogen atom of…

Q: Br2 но-

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Q: (f) Benzene + 3-phenyl-1-propene, H2SO4, heat -------> ? (g) Toluene +…

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Q: CH-CH, -ÇH- 24 H3C-CH-CH2 `CH3l 25 CHs -C,H5 26

A: The name for the given structures has to be given.

Q: 7. Choose the correct option. * 1 point NO2 AIC13 CI Major product + H;C CH3 H;C CH3 D) NO2 O NO2 B)…

A: Nitrobenzene does not give friedel craft reaction with acyl cation due to presence of nitro group in…

Q: fonowing cо ounds using H3C. CH3 HC CH3 CH3 CH3 CH2 H3C „CH2 CH ÇH HC CH3 H3C CH2 CH H3C-HC CH3 H2C.…

A: The IUPAC name of an alkane is determined in the following manner: The longest carbon chain is…

Q: Assign absolute configurations as R or S to each of the following compounds:

A: Since we only answer up to three sub parts, we'll answer the first three. Please resubmit the…

Q: H,C CH3 H3C- CH3 2,5-dimethyl-hept-3-ene Submit Previous Answers Request Answer X Incorrect; Try…

A: Correct name is , Trans-2,5-dimethyl hept-3-ene

Q: c. Hint: I'd sure use Newman projections or a model kit to predict this product! Br Ph CH3 (solvent)

A: Biomolecular elimination (E2) reaction:E2 reaction involves a one-step mechanism in which…

Q: Reagents Available a. CH2=CHCH2CI, AICI3 b. CH2Br2, OH c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4…

A: The given compound can be synthesized from catechol (1,2-benzenediol) using the reagents mentioned.

Q: Time left 0:31 Name these groups from left to right: CH3 CH3 H3C CH3 CH3 CH3 Oa isopropyl, isobutyl,…

A: The 1st group is isopropyl ,2nd is isobutyl and the 3rd group ia secbutyl

Q: H. Product b.) H. .D H. D. H' H. D. H. H. H. D.

A: Given reaction is an example of (4n+2)π electron cycloaddition reaction under heating condition.

Q: Complete the reaction map by matching the answers from A-E. SO3 Brz D HNO3 3, E C FeBrz CH3 CH2 CI…

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Q: (c) NO2 NH2 (CH3CO)20 pyridine HNO3 H2SO4 & heat NH2 O2N Br NH2 (d) NO2 3 H2 Ni catalyst А Br Br (e)

A: Stepwise synthesis is given below

Q: (a-b) (c-d) (e-f) OH CI CI HORE ? NH pyridine -OH HAM S CI LIAIH[OC(CH3)3]3 1. LIAIH4 2. H₂O+ 1.…

A: Lithiumaluminiumhydride is a reducing agent. It release hydride ion (H-). According to Q&A…

Q: 2. & ((A) (C) i + CH3 -C-H KOH A & i CH, - CH, - C – CH, – CHO major product: CH = CH₂ (B) (D) CH₂-…

A: Here the driving force for the reaction is to get relief from the bond starain that occurs in three…

Q: OBYJU'S Step -1 „OH +K - 12 H, - KBr

A: Organic chemistry is branch of chemistry in which organic reactant react to form organic products.

Q: For the reaction shown, add curved arrows for each step, then complete the statements. H. H3C, c=c°…

A: In addition reaction unsaturated compound is changed into saturated compound by addition new…

Q: Reagents Available g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 a. CH2=CHCH,CI, AICI3 b. CH2Br2,…

A: The answer is as follows:

Q: CH3 CI CH3 H20 (а) CH3 H20 (b) CH3-CH- -ċ-CH3 Br H20 Specify E and Z products (с) Нeat

A: E1 mechanism involves two steps. In first, slow step carbocation intermediate is formed. In second…

Q: Add curved arrows to the following polar reactions to indicate the flow of electrons in each: (a)…

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Q: H H;C, CH3 H3C- -CH3 OAc НОАС NEN -SO3 H H;C- N=N• SO3 CH3 proton transfer H3C -SO; H3C H Helianthin…

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Q: PCk H,-Pd BaSO4 CH;NO, 1,0 CH;O OCOC- CH;0 CO,H СНО NAOH (Rosenmund reduction) OCH3 OCH3 OCH3 OCH3…

A: PCl5 is a chlorinating agent. In Rosenmund reduction acyl chloride is reduced to an aldehyde.…

Q: a. H,O H,SO,, + Pt catalyst b. C2H5-CEC-H + H2 UV light C. CH:CH2CH2CH2CH3 Cl2 CH;=CHCH,CH,CH,CH; +…

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Q: 1. Sort the following molecules into the quadrant in the chart shown below that best describes them.…

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Q: Classify each addition as either syn or anti. Br Br₂ Rxn I CH3 Me HBr Rxn II Et Rxn II anti syn anti…

A: If the species add on same side then it is called as syn addition.  If the species add on opposite…

Q: 1. CO,+H,0 II. CH3-CH-O-CH2-CH3 25 °C OOH CH;CH,OCH,CH3 + O2 (slow) II. CH3-CH2-0-CH2-CH2-0OH IV.…

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Q: Name the following alkyl halides: CI CH3 CH,CH,ČCH,CH,CH;CHCH3 ČI CI H3C Br CH,CCH,CHCHCH,CH5 ČI 1st…

A: The name of the 1st compound is  3,3-dichloro-7-methyloctane. 3,3-dichloro-7-methyloctane

Q: Show hydrogen bonds and the dipole-dipole moments.

A: Hydrogen Bonding takes place when hydrogen atom of one molecule interacts with the electronegative…

Q: OH Br2 FeBr3

A: In this reaction Lewis acid FeCl3 polarises the bromine molecule. The phenol react to bromine give…

Q: 6. Draw curved arrows for the following reactions. Br CH3 + -> Br H3C H3C H H H H H-N-H H-N-H + :CI:…

A: Normally in organic chemistry, different type of arrows used for different purpose. Curved arrows…

Q: Determine the major product(s): : CH3 H2N :0: H3C no reaction CH3 HN но. :0: CH2

A: Ester is formed by the combination of alcohol and carboxylic acid. Alcohol gives H+ ion while…

Q: 6 f) -Br CI CI H3C- H3C- KI acetone CH3 OK CH3 CH3 -OH CH3 CH3CH₂ONa CH3CH₂OH

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Q: I. Dom stoucfural fr mulas of Strucfural H alkanı e 2 me thy! 2,3- dimethyl a methy! 3 methyl cyclo…

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Q: Br, CH,0 CH3 (A) - hv → (B) major product B is :- (1) -Br (2) ОСН, (3) (4)

A: A synthesis is the manufacture of chemical compounds by the reaction from simpler materials or…

Q: (a-c) (d-e) (f-g) OH ?? H₂O, H+ CI H₂O HBr OH ?? HIO4 ...H OH H H₂CRO4 O- +Na CH3Br

A: As per the bartleby guidline for answering the multiparts question, I can solve only first three…

Q: Draw the major organic product. H,C CH, Br H H3C CH3 H2 HC CH H3C- H H-Br H

A: HBr addition in alkene proceeds via formation of a stable carbocation. The mechanism is shown below…

Q: OCH3 OH CI O (2R,4Z)-4-chloro-2-hydroxy-5-methoxy-4-hepten-3-one O…

A: The rules for IUPAC naming is as follows  1. First we need to choose the longest carbon chain.  2.…

Q: Br -C CN H -Br NH2 H to H. CH3 d. 'CH2CH3 ČH,CH3 H. e. -H- ,NH ו . H3C bns Grcit CI f. CaCH3 H3C.…

A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…

Q: What is the product of the following reaction?

A: The reaction known as Claisen Condensation that occurs between esters containing a-hydrogens…

Q: Which molecule has the best leaving groue A.CHISH B CH3OCH3 C.CH3 NHCH3 D.CH30H E.CH3 CH2 SCH3 CH,…

A: More is the acidity of leaving group , better is leaving group .

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.