HO. 1) H-C=C Na Br 2) SiaąBH 3) H2O2, NaOH, H20 H. 3 4 2.

Q: H,SO4 (A) -OH но 180° K,Cr,0,, H,SO4 (B) он (F) (E) (D) (C) \KMNO4, NaOH, Hz0 PCC, pyridine sodl,…

A: Since you have asked a question with multiple sub-parts, we will solve the first three sub-partts…

Q: 10) o Na ct, ce to -7 1) CHz 12) 6CH = CH2 Na BHy /$3 CoH 13) Oo Hcl HI 14) t 15) ø CH = CH øt cHz E…

A:

Q: OH LIAIH, CH,MgBr HO 2. H,0* 2. H,O* H,O* Answer Bank CH,OH CH,CO, Na -78 °C NaCI CH,ONa CH,NH,…

A: There is some blank box in the answer bank. So, you can put (CH3)2CuLi in the answer bank.

Q: F CH3 H OH H Br Br when More Br Br CH3 Br HO NH₂ Br Ch NH CH3 ▸

A:

Q: A) 1) Hg(OAc)2, H2O HO 2) 3) NABH4 B) 1) Hg(OAc)2, H2O 2) NaBH4 но

A:

Q: (d) HCIO + CH;NH2 = CH;NH + CI0 (e) CO + H2O = HCO; + OH (f) CH3COO + H2O = CH;COOH + OH

A: In reaction which release H+ that will be acid and which gain H+ that will be base. Conjugate of…

Q: 15. CH2OS 11. C2H4 H. 12. CO2 16. SİH3CI 13. CH2O 17. SiH;P H. CHO 14. CHN 18. H3OP

A:

Q: OEt (3) ? NaOEt, ELOH

A:

Q: 3.) Br CH3 4.) H3C- H2N

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: PHCHO Br2, NaOH кон, heat (a) tBu (b) Ph Me Me NaOH, H2O2 LIAIH4 NME2 (c) (d)

A:

Q: 1.) HAI(Bu), or DIBAL-H 2.) H,0", H,0 CEN: H. R' H. 3 3 1.) HAI('Bu)2 or DIBAL-H 2.) H,O*, H,O…

A:

Q: Question attached

A: In the presence of strong acids, such as sulfuric acid and heat, alcohol dehydrates to an alkene.…

Q: Each of the following reactions has been described in the chemical literature and gives a single…

A: Hey, since you are posted a question with multiple sub-parts, we will answer first three sub-parts.…

Q: Br Br- -CH-CH;, НО -H ОН CH2CH3 ŅH2 CH CH3 F- -CH; NH2 Cl キ, F НF Cl- -H H2N. Cl H2N- -CH3 НС Н H

A: Explanation- 1) Disteriomers- having different configuration around the more than one carbon atom .…

Q: но, N' H HO, HBr 10 -8 10 16 H. H HO TH

A: The solution is as follows:

Q: (а) Cl НО (b) Н—он (с) H' Br CH, CH, н он CH,Br CH,Br CH, () Н— Br -H- (е) Н— Br ) Н- -Br H -Br Br H…

A: Since you have posted a question with multiple sub- parts, we will solve first three sub- parts for…

Q: H3C CH3 H2O H2SO4 Br HO ELOH Br SH NaOH HO 1) NaH 2) BRCH,CH,F OH H2SO4 LOCH3 1) LIAIH4 2) H3O* NC.…

A: The detailed mechanism provided  in attach image

Q: Draw the products of each reaction.

A: The reaction of Chlorobenzene with sodium amide in the presence of liquid ammonia gives Aniline.…

Q: HO OH H. Br CH3 H3C CI H. ICH CH3 of CH3 H. Sli

A: Enantiomers which are mirror image to each other or complete configuration should change (R,S)to…

Q: Br NACN A H30* В SOC2 1. (CH32CULI E 2. H2О 1. LIAH4 2. H20 CH3OH, H* РСС 1. DIBAH-H F 2. H20 1.…

A: As the question ask to find only k l and m so I am focusing finding them only .that can be found by…

Q: 1.NGNH2 -7 2. CH3 CH2I a. mo b. m H2, Lincllar -) 1.03 cl. H*, Hz0, Hge-> 1. R2BH 2. Ha0, O4-, H20

A:

Q: он LIAIH, CH,MgBr HO, 2. H,0* 2. H,0* H,O* Answer Bank CH,OH -78 °C NaCI CH,CO, Na CH,ONa CH,NH,…

A:

Q: a) Ph :O: CH 3 Br₂, H₂O Brz -OH 1. LDA, -78°C 2. A Br 1. LDA, 20 °C 2. -Br

A:

Q: Br HO EtO₂C CO₂Et C5H11 NaOEt / EtOH 99% CO₂Et H₂/Pd-C C5H11 8 OH Br 10 OH EtOH 72% HO NaOH HO OH 11…

A:

Q: ÇOOCH3 CH3. (CH)2СHNH2, CH;OH, A 1. КОН, Н2О 2. H*, H,O CH;CH, COOCH3 1. ether, 20 °C 2. H", Н,О…

A: There are some  reactions which are shown above . we have to draw the product of the above reactions…

Q: In each equation, label the acids, bases, and conjugate pairs:

A: Lowry Bronsted acid- The substance that donate proton during chemical reaction called as Lowry…

Q: CH3 H3C H30", A H;CH;CO OCH,CH3

A:

Q: Br NaNg 17 Acetone NH2 NH2 A. B. 18. oH HO HO B. C. A. N.

A: 17.  Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic…

Q: Me NABH, i) MEOH i) CH3NH2 ii) ii) LIAIH4 iii) H20 HO. Br i) NaCN iv) HD D ii) H3O i) Base E v) OEt…

A:

Q: -CH2CONH2 1. Br2, NaOH

A:

Q: Mg H20 H;C-C-I CH3 Et,0 KCN `CI H3C CH;0¯ Na* H;C-CH,-Br

A: Grignard reagent (RMgX) can be easily prepared using alkyl halide in the presence of magnesium…

Q: е. d. 2 eq. HBr H2O, H,SO4 HgSO4 H, BH3 Pd/BaSO, H,O2, OH Li conc. KMNO, NH3 H,O H2 O3, -78 °C Pd/C…

A: The answer is given as follows

Q: d) :OCH d) HÖ e) CrO3 (excess) e) HO H2SO4, H20 HÖ: f) f) -P=CH2 3

A: The given reactions are,

Q: HO ∞ H Br KMnO4 NaOH 0 °C 1. KMnO4, NaOH, A 2. dil. H₂SO4, H₂O 1. KMnO4, NaOH, A 2. dil. H₂SO4, H₂O…

A: Here we have to predict the major products formed in the following given reactions.

Q: LOH [1] SOCI, f. [2] CH3CH,CH,CH,NH2 [3] LIAIH4 [4] H2O д. НО OH + -NH2 h. (еxcess)

A: In presence of SOCl2 , acid chloride is formed.  Then amine acts as Nucleophile and carry out…

Q: товокза Ph H₂N О А О в О с O D D HO NH OH NH O В C HO. Ph. NH OH

A: The reaction in the question is the reaction between an amino acid , alanine and benzyloxycarbonyl…

Q: 19 H3C- -CH, CI 20 Br Br HC Ec- -CH-CH-CH,-CH, 21 HC-C CH

A: The organic compounds are named according to the IUPAC nomenclature. It is done according to some…

Q: What are the final products for these reactions? *mechanisms not necessary

A: The final products of the given reactions can be written as : The reaction of alkyl halide with KCN…

Q: Give the IUPAC name for each compound.

A: IUPAC (International union of pure and applied chemistry) has given the method of giving specific…

Q: Fill in the expected organic substances:

A: The reaction of alkyl halide with hydroxide produces alcohols by SN2 reaction. The alcohol so formed…

Q: H H H H -С -О-С-С-Н НН Н НН Oa CH3 H3C НННН 111 н-с-с-с-с-OH - НННН SH CH3 CH3 Н Н нннно IIII 0…

A:

Q: Fol (u) (v) (w) (y) i CI H + CH3NH₂ CH₂MgBr A Ph H₂NNH₂, OH Ph- Ph 1. HOCH₂CH₂CH₂OH, H* 2.CH3MgBr 3.…

A:

Q: 9) H,C. 1. LIAIH 2. H3O* h) 1) CHsMgBrléter anh. 2) H3O* i) H3O /calor

A:

Q: -OH A. HCl На B H Br 2 C. SOU ₂ D. POCI₂ CI t

A: The above reaction is a transformation of alcohol to haloalkane( here chloroalkane). The reaction is…

Q: Br 1. Mg, ether 2. Со2 (a) 3. Н.О, Н OH H+ (b) HO, (с) NaHCO3 HO. ? HO. CI (d) K*OH (e) HO, 1. NaCN…

A: We have to provide the product or reagent for the following given transformations as follows in step…

Q: 1. LDA, - 78 °C 2. Cals-CHz-Br в D

A:

Q: i) H. .CO2H 150°C ? + H20 90% H `CO,H Maleic acid ii) (CH;CO),O + (CH3)½C-OH ÇOOCH3 i11) + OH NAOH ?…

A:

Q: K H NaOEt, E1OH NC. CN NaOEt, EtOH H H. M NaOEt, EtOH

A: 1) Reaction of an active methylene compound with carbonyl compounds is called Knoevangel…

Q: LIAIH, CH,MgBr 2. H,0* 2. H,0* H,0* Answer Bank CH,OH -78 °C NaCI CH,CO, Na CH

A: Many reagents can be used for this conversion i.e; Acid chloride into ketone.

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.