Q: Name the following ethers: CH3 CH3 (а) (b) -OCH2CH2CH3 CH3CHOCHCH3 (с) LOCH3 (d) LOCH3 Br
A: According to Bartleby guideline I have done only the first question sub parts.
Q: Which reagent would be best to convert cyclohexanol into chlorocyclohexane? O HCI AICI3 C12 O SOCI2
A: Which one of the following is correct
Q: CH₂CH3 (b) CHCH3 CH3 (c) H3C.... CH3
A: Ethers form by using alcohol and this method is known as williamson ether synthesis. Last ether is…
Q: Prepare each compound from cyclopentanol. More than one step may be needed.
A: Organic synthesis processes are used to prepare different organic compounds by organic reactions…
Q: Two diastereomeric sets of enantiomers, A/B and C/D, exist for 3-bromo-2-butanol. CH3 HO--H CH3 HO…
A: The given molecules are represented as follows:
Q: Give the IUPAC name for each ketone: CH3 (CH3)3C. b. c. (CH3)3CCOC(CH3)3 a. Name the following…
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Q: 1.) Which is the structure of (R)-2-chlorobutane? CH C CH, CHCH, H,C C CH H,C a CH,CH, H,C CHCH, II…
A: Assymetric Carbon is the carbon which has all four different group around it. A Stereogenic center…
Q: . Name this ether correctly. CH3CH2CH2CH2-O-CHCH=CHCH3 ČH3
A: IUPAC rules : Ethers name should be "alkoxyalkane" , lower carbons chain should be alkoxy side ,…
Q: /hich of the following compounds is an aldehyde? -0-CH3 I. IV. CH3 П. V. III. -OH- Select one: O a.…
A: In organic chemistry most of the compounds have different functional group. These functional groups…
Q: Reagents 1. Li(CH3)2Cu 2. H30* 1. Li(CgHs)2Cu 2. H30* 1. Li(CH2=CH)2Cu 2. H30* a i 1. NaBH4 f CH212…
A: This question is demanding the basic knowledge of organic reagents which can be used for the…
Q: Give an IUPAC or common name for each compound.
A: (a) The functional group present in the given compound is acid chloride. The parent chain consists…
Q: Draw two different routes to each of the following ethers using a Williamson ether synthesis.…
A: Williamson ether synthesis is the synthesis of ethers from alkoxide ( deprotonated alcohols) and…
Q: Br - OCH3 Нeat
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Q: 12 & 1.4-addition products from ether cleav Br HBr 2 HI Br Cl,2) (c) (d) OH (1) Na H2SO4 (2) C2H5-Br…
A: In Williamson ether synthesis method, a metal alkoxide ion undergoes reaction with primary alkyl…
Q: NaH ND CH OTs MCPBA 8) CH,CI, NaOH HO KOH 人人l NAOH
A: MCPBA prefer to do epoxidation this reagent is electron deficient in nature thus it attack on…
Q: Prepare each compound from cyclopentanol. More than one step may beneeded.
A: (a) The reaction of alcohol with HCl in the presence of catalyst ZnCl2 leads to formation of alkly…
Q: Rank the following alcohols in order of increasing reactivity toward dehydration with H2SO4. HOH HO…
A: Most interesting question
Q: Identify the major enol form of the molecule below OH ОН ОН OH A. В. С. D. (A) (B) (C) (D) O O O
A: Tautomerism is a special type of functional group isomerism in which both the functional group are…
Q: Which of the following compounds is an enol of compound X drawn below? Compound X QH ОН A. B. C.
A: In organic chemistry the chemical equilibrium that exists between keto form and an enol form is…
Q: name the following ether using (Non-IUPAC) CH3CH2CH(CH3)OCH2CH2CH3
A: Ether group ( R - O - R' ) In the Ether group , the Oxygen atom is bonded by the two sides by the…
Q: 3. Label each acetal, hemiacetal or as an an ether. -CH3 CHs CH3 C. CH3 -OCH3 d. f. e.
A: Acetal : Acetal is any diether of a geminal diol. Hemiacetal : Hemiacetal is any monoether of…
Q: 5. Identify the structure of compounds A to E below 1) 1eq. Br2 Mg A B FeBr3 (major product) Ether…
A: Step 1: Ethyl group is an electron releasing group that is connected with benzene and gives the para…
Q: \Q3 Name the following heterocyclic ethers (a) إجابتك Name the following heterocyclic ethers H O.…
A: (a.) 3,4-dihydro-2H-pyran (d.) 2,3-diethyloxirane (f.) 3-bromo-2,2-dimethyloxetane
Q: Which of the following can hydrogen bond with water? A. CH3CH2CH3 B.H2 C.HSCH3 D.NH4+
A: For any molecule to make hydrogen bond with water, it should be either a hydrogen bond donor or…
Q: Reagents Available a. benzene/AICI3 d. H20, H2SO4 g. LIAIH4 j. PBr3 e. H2, Pd/C f. K* OC(CH3)3 i.…
A: The structure of the butanoic acid, butanal, and N-methylpentanamide is as follows:
Q: What is the IUPAC name of the compound below? Select one: a. (Z)4 bromo-S-ydlopropyl.3-hexenoyl…
A: The given compound contains a six-carbon atom chain and acid bromide functional group, hence the…
Q: What is the most proper name of the following ether? OCH3 a. (25,3R)-2-methoxy-3-methylpentane b.…
A: Write proper name of the given ether ?
Q: Part 1: Draw the organic product of the reaction. + OCH(CH3)2 view structure Part 2 out of 2…
A: symmetrical ether - substituent on both side of oxygen is same
Q: Identify the reagents a-e in the following scheme: CH3 OH CH3 -CH3 d. a CH3 OCH3 -CH3 H.
A: Grignard reagent reacts with ketone to produce secondary alcohol Alcohol reacts with alkylhalide in…
Q: Identify the needed reagents in the following scheme: CH3 Br он CH3 CH3 CH3 CH3 С. b. а.
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Q: Give a systematic or common name for each compound.
A: (a) (b) (c) (d)
Q: 2) Name the following ethers
A: IUPAC name of ether is alkoxy alkane, where alkoxy is used for small alkyl groups connected with…
Q: 1. Give the IUPAC name for the following compounds, and/or include R/S configurations in the name:…
A: Answer:- We are asked to give the IUPAC nomenclature with R/S configuration. We would use…
Q: Give the IUPAC names (including E,Z and R,S designations) for the following compounds: (a) (b) Jay…
A:
Q: What is the most proper name of the following ether? OCH3 a. (25,3R)-2-methoxy-3-methylpentane b.…
A: The IUPAC name of the following ether is
Q: Part 3: Name the following ethers. Use-oxy if g Name: Name: Name:
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Q: 33. Consider the reaction scheme below: CH;CHO A CH;MgBr B CH;CN CH3COOH 1. Dry ether 2. H;0* E…
A: Answer:- This question is answered by using simple concept of chemical reaction of organic compounds…
Q: The major products of reaction of ethyl cyclopentyl ether with HBr are: Select one: O a.…
A: Ether consists of electron-rich O atom which can be attacked on electron-deficient atoms like H+.…
Q: (2) (1) I CH3 CH2 CH3 This ether can, in principle, be synthesized by two different combinations of…
A: This ether can be prepared by reaction between sodium alkoxide and alkyl halide. This is SN2…
Q: When alternative pos CN (a) Butyl sec-butyl ether (e) (i) cis-4-Isopropylcyclohexanol H CN (j) (b)…
A: The below pictures gives the synthesis methodology
Q: Two naturally occurring compounds that contain stable cyclic hemiacetals and acetals are monensin…
A: Carbonyl compounds and imide generally undergo a process called tautomerization. Tautomerization is…
Q: Write the common name for the ether. CH3CHOCHCH3 I I CH3 CH3
A: Ethers consist of two alkyl group directly connected to an oxygen atom. These alkyl groups can be…
Q: Des Martin Periodinane CH CH pH 45 10. H. KCN HCN CH-CHCH, THE ether 2. H0
A: All the given reactions involve the conversion of one functional group into other functional groups…
Q: 5 Compound X IS a monocyclic and has molecular formula Cy Ho CID. The IR spectrum for compound X…
A: (5) C4H5ClO DBE = 4 + 1 - 5/2 - 1/2 = 2 IR 1790 cm-1 : C=O stretching (presence of carbonyl group)…
Q: 4 What is the proper IUPAC name for the structure shown below? NH₂ am) and
A: Rule of IUPAC-1) Longest chain as parent chain.2) Numbering start from those side where more prior…
Q: Name the following ethers: (а) CH3 CH3 (b) OCH2CH2CH3 CH3CHOCHCH3 (c) OCH3 (d) OCH3 Br
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Q: Which of the following molecules will have two mirror-image forms? a.1,2-chloroethanol…
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Q: Explain why tetrahydrofuran has a higher boiling point and is much more water soluble than furan,…
A: The physical properties of any molecule can be easily determined by applying the facts of the Vander…
Q: 2.1. What is the most proper name of the following ether? a. (Z)-5-oxyethyl-1,1-dimethyl-3-ene b.…
A: To write the most proper IUPAC name of the below compound
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- = TriCor (fenofibrate) is used to lower cholesterol levels in patients at high risk of developing cardiovascular disease. Identify the circled functional groups in TriCor. $ 4 R F V ester % :O: 5 G Search or type URL T G tv B ether 6 MacBook Pro Y aromatic ring H & 7 N ether U :0: J * 00 8 M aromatic ring I K ( 9 < V- O ) O L aromatic ring carboxylic acid aldehyde A P Answer Bank 11 P L command option ketone { [ amide + ester = ether } 1 delet .app.101edu.co uTube Maps 35 80 F2 F3 F4 ! 1 ion Q A L N 2 W S X H 5 command #3 E D C Be dc Ho [S Ma Question 32 of 48 What is the correct IUPAC name for the compound below? $ 4 R F do 5 % V F5 -4 T X G D 6 MacBook Air F6 Y 7 F7 U H BN W * A) 3-propyl-4-ethylheptane B) isooctane C) 3,4-dipropylhexane D) 4,5-diethyloctane E) None of these are correct ▷▷ F9 DII F8 8 T J M ( 9 HG 17 C Sc UO NO K ) O L H 7 L F10 [ {T A ? 1 command option Et P F11 + 11 WL Ba7 Identify the functional group and the IUPAC name for each of the three compounds in the reaction below: H₂SO4(aq) Compound 1 CH₂COOH (1) + CH₂(CH₂)₂OH(1) I || || Functional Group carboxyl hydroxyl Ester linkage + CH3COO(CH₂) CH₂(1) + H₂O(1) IV III IUPAC Name → + +
- Home apter 11 Homework oblem 11.26 - Enhanced - with Feedback rch You may want to reference (Pages 376-378) Section 11.5 while completing this problem. Give the IUPAC name for each of the following. 27 6354 (r BREW - BE GOOD, a Azel Tov DISH - "IA GU Show THIS INSTE SHA Schoond ystane Part A H₂C=CH-CH2-CH3 Spell out the full name of the compound. Submit Part B Submit CH3-C=C-CH₂-CH-CH3 Spell out the full name of the compound. Part C Request Answer 72 BAKERY Request Answer hp -2221 CH3 51-19-145 PALM BCH tion, Inc. Address erbert Epstein 14773 Cumberland D DELRAY BEACH, FL Herber12. What is the IUPAC name for the following compound? H CH, O H Н-С—С— С—С-Н нн H A. 2-methylbutanone В. 3-methylbutanone С. 3-methyl-2-oxobutane D. 2-methyl-3-oxobutaneDraw the structures of the following molecules: (a) trans-l-Bromo-3-methylcyclohexane (b) cis-1, 2-Dimethylcyclobutane (c) trans-1 -tert-Butyl-2-ethylcyclohexane
- Alcohols undergo an oxidation reaction to yield carbonyl compounds on treatment with CrO3. For example, 2-tert-butylcyclohexanol gives 2-tert-butylcyclohexanone. If axial OH groups are generally more reactive than their equatorial isomers, which do you think reacts faster, the cis isomer of 2-tert-butylcyclohexanol or the trans isomer? Explain.+ C 2 F2 W S What is the correct IUPAC name for the compound shown here? C3 # 3 F3 e T Oll F4 $ 54 D f F5 % 5 hex ethyl M t 3- C Question 24 of 49 F6 A 6 2- 5- 1- hept propyl cyclo methyl ( DELL y C F7 & 7 u F8 8 F9 9 F10 0 0 8 F11 F12 B Р Mar 24 L + 11 delHgSO4 H2SO4, H20 1T (1) Br H2O2, NaOH 10 NaNH2 BH3, THE H =H 1S NH3 H20 HCI (1 equiv.) diethyl ether 1V 1W Br2 (m) MgBr (H,C=CH),CULI NaOCI ТСРВА > 1X 1Y > 1Z CH3COOH 1AA diethyl ether SoCI2, pyridine diethyl ether 1AB
- Which of the following is not another representation for 2-methylbutane? H H₂CH₂C+CH₂ CH₂ 1 Multiple Choice CH₂CH₂CH(CH₂)2 111 HH H-C-C-H H₂C- CH₂ CH₂ IVW What is the correct IUPAC name for the compound shown here? C # 3 e Oll 4 F4 2,2- 2- LL % de in r O 5 Question 11 of 49 t tetra ISO sec- di Σ F6 3- 4- 2,3- 3,4- < 60 tri GO DELL A y F7 & 7 4 u F8 * CO 8 F9 ( 9 F10 0 0 F11 Р 8 F12 Mar 24 E [ 8 deleteCH;CH3 Br CH3 If you take the above compound, and place an ISOPROPYL group on the carbon of the ring directly between the bromo and methyl groups, you will have a ring with four groups, all on different neighboring carbons. The correct IUPAC name of this new compound would be (including numbers and proper punctuation when required):