Q: Only question 64
A: Answer IUPAC and common name of the given compound
Q: H CH-CH2 CH:CaHs Br H H3C H3C CH=CH2 H Br CeHsH2C
A: Graph2 has highest energy at given energy profile diagram thus the conformation having lowest…
Q: O CH3 CH2 CH = CH2 + HBr H2S04 ( CH3 C = CH2 + Ha0 CH2C12 O CH3 CH = CH2 + Cla
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Q: CH3 CH(CH32 H3C, H H
A: The structure of the above given compound can be drawn from the Newman projection given above,
Q: NH2 C-CH-CH,-CH,-CH3-NH,
A: Selectr the longest principal carbon chain which has 5 carbon in this molecule.NH2 group behave as a…
Q: Draw each stereogenic center using a Fischer projection formula.
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Q: CH2 H3 C CHz CH3 CHz. CHZ H3 C CHz CH2 CH3
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Q: 3 С вс — сHа— сH —с — сHz—С 3с — соо—CH CH2OH H3C – C-CH3 CH3
A: The compound given is,
Q: H,N CH2CH3 CH,CH,NH2 b)
A: Nomenclature: With he help of iupac nomenclature we are enable to study the organic structure…
Q: CH3 H3C CH3 H3C
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Q: H3C. OH H3C. H3C но. CH3
A: Step 1 Dehydration. Step 2. Ozonolysis of alkene to give aldehydes. Step 3. Reaction of aldehyde…
Q: H,C HN-CH2 CH3 H2 C HC H2 CI H3C H2 CH.
A: The reaction is a nucleophilic substitution reaction.
Q: Name the following compounds using R,S designations:
A: The priority to the substituents attached to stereogenic centers is given by following these rules:…
Q: CH2 CH3 e) CH3 CH=CH CH, ChH CH
A: 2,3-dimethyl-cyclohexan-1-one (i) Identify the number of carbon atoms in ring. Here the number of…
Q: H2SO4 H3 Co- CH30H
A: Note: Since you have posted multiple independent questions in the same request, we will solve the…
Q: H2 H. H3C H,N-CH3 CH3 wwww Br CH
A:
Q: CH3CHCH,CH2OH K2C1207 CH3 H2S04
A: Answer:- This question is answered is by using the simple concept of oxidation of primary alcohol to…
Q: CH3-CH2 C-N-CH3 + H H. H.
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Q: а. Sv1 H,C CH CH, Br H,C-C-CI CH II III b. Sx2 CH, CI H,C-C- CH;CH,CH2CI CH;CH2CHCH3 CI ČH3 II III
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Q: What is the major product of each of the following reactions?
A: The complete chemical equation for (a) is shown below.
Q: a O₂N. HO C e O₂N SO3/H₂SO4 CHO CH3 Br₂/A COCH2CH3 Zn/ (Hg) / HC1
A: a) The 2- nitrophenol is a process of heating with fuming sulphuric acid (H2SO4 +SO3) to…
Q: CH3 CH CH H3C CH3 CH2
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Q: CI H3C, HO H3C. HCI + H2O + H3C CH3 H3C CH3
A: The above Reaction is between Alcohol and the Hydrogen Halide This is the type of nucleophile…
Q: CH,CH3 H3C. .CH3 НС—С—Br H ČHĄCH3
A: Regioselctive reaction in which the structural isomers formed in unequal amount. The regoselectivity…
Q: 6. 5. 4. CH OH H3C. CH3 H2C CH3 CH3 CH3 CH3 HO CH3 H3C
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Q: H CH3 CH3 H3C. H3C `CH3 CH3 DC HC ČH3 ČH3
A: Introduction: This is an example of cyclopropene to cyclopropene rearrangement. Cyclopropene is a…
Q: CH3 H3C (1) H2 H2 -CH3 H3C (2) fu CH
A: 1.
Q: CH3 HO H3C CH3 CH3 H3C
A: The question is based on the concept of chemical conversions. we have to convert the reactant into…
Q: CH3 CO2H C-C CH2OH H. CN C-C CH2NH2
A: The question is based on the concept of alkenes IUPAC naming. we have to identify which of the given…
Q: CH3 H,CH,C-C-X ČH,
A: Homolytic cleavage leads to the formation of free radicals. Heteroytic cleavage leads to the…
Q: H3C H CH3 CH3 CH3 H
A: The given saw-horse projection formula of 2,2-dimethylbutane can be drawn in Newmann projection…
Q: „CH2 CH2 H3C CH2 f. H3C, CH CH2 CH3 ČH3
A: IUPAC naming of a compound is done in such a way that the chain which contains the highest no. of…
Q: What is each compound’s systematic name?
A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…
Q: H3CH2C NEN-C CH2 N=N=CH
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Q: CH3 Br H3C- H3C. он H3C CH3
A: IUPAC Name of the given compounds.
Q: >CH3 (CH2)22 CH CCH2)18 CH3 H2O
A: Acid catalysed hydration of alkene to give alcohol as the product. It is an example for…
Q: For each of the reactions indicate which reactant is the nucleophile and which is the electrophile.
A: Since your question has multiple sub parts, we are solving only first three sub parts for you .If…
Q: он CH3 CI NH2 H,N. H CH3 CH3
A: The molecules whose configuration is not superimposable with its mirror image are chiral. A…
Q: CH,CH3 AICI, + H3C k.
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Q: CH3 :C CH3 H3C-CH2 CH3 CH3 CH,CH3 ČH,CH3
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Q: cHs a) cH3-C=CH2 B% jthae | cHs b) CHs-c=cH_ Og/2h
A: The products for the given reaction has to be given.
Q: *.4 We CH3 H3C- CH3 -CH3 H3C
A: I u p a c name of given compound Main functional group is alkyne
Q: „CH3 CH CH "CHs „CHy CH, HyC
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Q: (а) CH3 (b) + H3C. CH3 (с) CH3 H3C. (d) CH3 (е) H3C. CH3 + + + +
A: One of the given reactant is a conjugated diene and the other is dienophile (substituted alkene).…
Q: CH3 H* CH3 H3C OH
A: Alcohol gives dehydration reactions when they react with acid to form alkene at 180oC. The reaction…
Q: а. N; b. H3C CHCH2 H3CO CH2NH2 C. HN
A: E and Z configuration of double bonds based on group priority. It is Z if the high priority group…
Q: NH3 H3C CH H3C CH3
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Q: (CH3),CH (CH3);C' CH;CH,
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Q: H2C=CH2 + KMNO ?
A: Given :- H2C=CH2 + KMnO4 → To determine :- major product formed in above reaction
Q: CH3 N . H2SO4 . H2O H. CH2OH
A:
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- Compound p,c6h14O does not react w/sodium metal,doesn't discharge the color of Br2 in ccl4, the H-NMR spectrum shows 2 signal,a 12H doublet at 1.1, and a 2h sextet at 3.6. Propose a structure for this compound,p.Compound A (C6H12O2) reacts with water, acid, and heatto yield compound B (C5H10O2) and compound C (CH4O).Compound B is acidic. Deduce possible structures of compounds A, B, and CAn optically active unknown compound B, whose molecular formula is C6H10, reacts with H2/Ni produce compound C, whose molecular formula is C6H14. Compound C is optically inactive. What are the structures of compound B and C ?
- Arrange the following compounds in the increasing order of reactivity towards Conc.HNO3 & Conc.H2SO4 1. Benzene 2. Chlorobenzene 3. phenol 4. Toluene 5. Nitrobenzene 5,2,1,4,3 5,1,2,4,3 5,1,4,2,3 1,2,3,4,5The molecule shown is used in the chemical industry to dilute hydraulic fluids. Draw the major organic product when the molecule reacts with thionyl chloride. Include wedge‑and‑dash bonds to show the stereochemistry of the product.A compound C4H11N is known from its reactivity andspectroscopic properties to have no hydrogen atomsattached directly to the nitrogen atom. Write all structuralformulas consistent with this information
- Compounds A and B are isomers having molecular formula C5H12. Heating A with Cl2 gives a single product of monohalogenation, whereas heating B under the same conditions forms three constitutional isomers. What are thestructures of A and B?b. In a strongly basic solution, the starting material again converts into a molecule with the molecular formula C6H12OC6H12O. but with a completely different structure.Three isomeric compounds, A, B, and C, all have molecular formulaC8H11N. The 1H NMR and IR spectral data of A, B, and C are given below.What are their structures?
- Compound A has a molecular formula C6H12 , and has the following; 2 secondary carbons 2 primary carbons A plane of symmetry Compound A is treated with H2 and Pd to give compound B. Compound A was treated with ozone and gave 2 equivalents of compound C with the formula C3H6O.Compound A was then treated with CH2I2 and Zn to form Compound D, which has two stereocenters and is meso. What are the structures for compounds A-D? Compound A and Compound C IR spectrum are given below. What is the structure of Compound A?Rank the following groups in order of decreasing priority. −F, −NH2, −CH3, −OHCompound A has the formula C5H10O that is produced by oxidation of a conpound that has the formula C5H12O. Compound A has an IT spectrum the has an absorbance at 1700 cm^-1 and no broad absorbance from 2500-3500 cm^-1. The 1H and 13C spectrums of Compound A both have 4 peaks. What is tbe structure of Compound A? Thank you for the help!