Interpretation:
The 3-D formula of the products when 1-methylcyclohexene reacts with the given reagents is to be written. The location of deuterium or tritium atoms in each case is to be designated.
Concept introduction:
Electrophiles are electron-deficient species, which has positive or partially positive charge. Lewis acids are electrophiles, which accept electron pair.
Nucleophiles are electron-rich species, which has negative or partially negative charge. Lewis bases are nucleophiles, which donate electron pair.
Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a
Elimination reaction: A reaction in which two substituent groups are detached and a double bond is formed is called elimination reaction.
Addition reaction: It is the reaction in which unsaturated bonds are converted to saturated molecules by the addition of molecules.
Hydroboration-oxidation: An organic reaction in which the double bonds of
When
Want to see the full answer?
Check out a sample textbook solutionChapter 8 Solutions
Organic Chemistry
- Name the type of reaction; then predict the products. Make sure the reaction is balanced.arrow_forwardBent (D) Trigonal pyramidal 5. A student wishes to prepare ethyl acetate from the reaction of ethanol and acetic acid. To be successful, this reaction requires (A) an acidic catalyst. (C) an oxidizing agent. (B) a basic catalyst. (D) a reducing agent. 6. Which alkyl halide reacts most rapidly with aqueous sodium hydroxide solution? (A) CH₂Cl (B) CH₂I (C) (CH3)3CCH₂Cl (D) (CH3)3CCH₂I 57. How many isomers are there with the formula C6H₁4?arrow_forward(1) Predict the outcome of the addition of HBr to (a) trans-2-pentene, (b) 2-methyl-2-butene, and (c) 4-methylcyclohexene. How many isomers can be formed in each case?arrow_forward
- 5B In the following reactions, mixtures of alkenes and ethyl ethers are formed. Draw their structures. Explain which is or are likely to be the main product(s) in each reaction. In case of formation of two isomers of alkenes, explain which is formed in greater proportion CH3 CH3 H3C-C H -Br CH3 EtOHarrow_forwardWhich products are formed when hydrobromic acid is added to (a) trans-2-hexene, (b) 2-methyl- 2-pentene, and (c) 4-methylcyclohexene, and how many regioisomers can be formed in each case?arrow_forwardIdentify the following reactions as either SN1, SN2, E1, or E2: (a) Br CHCH3 CH=CH2 кон (b) Br OCH3 .CHCH3 .CHCH3 CH3OH Heatarrow_forward
- 4 But-2-enal, CH₂CH=CHCHO, is a pale yellow, flammable liquid with an irritating odour. (a) But-2-enal exists as two stereoisomers. Draw skeletal formulae to show the structure of the two stereoisomers of but-2-enal. (b) (i) Describe a simple chemical test that would show that but-2-enal is an aldehyde. (ii) Explain why this test gives a different result with aldehydes than it does with keton (c) But-2-enal also reacts with sodium borohydride, NaBH4. (i) Identify the organic compound formed in this reaction. (ii) State the type of chemical reaction occurring. (d) Precautions must be taken to prevent but-2-enal catching fire. Construct a balanced equation for the complete combustion of but-2-enal, C₂HO.arrow_forwardWrite an equation to show the proton transfer between each alkene or cycloalkene and HCl. Where two carbocations are possible, show each. (a) CH,CH,CH=CHCH, (b) 2-Pentene Cyclohexenearrow_forward嘉伯麗 1. Name the following alkenes, and predict the products of their reaction with (i) KMnO4 in aqueous acid and (ii) KMnO4 in aqueous NaOH: (a) (b) 2. Draw structures corresponding to the following IUPAC names: (a) 3-Ethylhept-1-yne (b) 3,5-Dimethylhex-4-en-1-yne (c) Hepta-1,5-diyne (d) 1-Methylcyclopenta-1,3-diene 3. Draw and name all the possible pentyne isomers, CsH8. 4. Predict the products of the following reactions. Indicate regioselectivity where relevant. (The aromatic ring is inert to all the indicated reagents.) CH=CH2 Styrene Pd (a) Styrene+H2 ? (b) Styrene+Br2 → ? NaOH, H2O (c) Styrene+HBr → ? (d) Styrene+KMnO4 5. Suggest structures for alkenes that give the following reaction products. There may be more than one answer for some cases. H₂Pd catalyst (a) ? (b) ? Br2 in CH2Cl2 HBr (c) ? 2-Methylhexane 2,3-Dibromo-5-methylhexane 2-Bromo-3-methylheptane CH3 HO OH CH3CHCH2CHCHCH2CH3 (d) ? KMnO₂OH- H₂Oarrow_forward
- A hydrocarbon C5H12 gives only one mono-chlorination product. Identify the hydrocarbon.arrow_forwardWhat is the structure of the major product(s) formed when 2-methyl-1-butene reacts with (a) bromine (b) bromine in water (c) bromine in NaCl solutionarrow_forwardDraw the skeletal structure of the following organic molecules. (i) 4-chloropentanal (ii) 2,3-dimethylbutan-1-ol (iii) CH3CH(OH)CH₂CN (you can leave the nitrile group as -CN) Name the organic molecules shown below. (i) (CH3)2C=CHCH₂CH3arrow_forward
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning