(a)
Interpretation:
To draw the product formed when 1-ethylcyclohex-1-ene reacts with HI.
Concept introduction:
The reaction of hydrogen halide like HCl, HBr with an
(b)
Interpretation:
To draw the product formed when 1-ethylcyclohex-1-ene reacts with
Concept introduction:
The process hydrogenation is the addition of hydrogen to a double bonded compound in presence of catalyst like Nickel, Platinum etc. The product of this reaction is a saturated compound that is, no single bond present. Therefore,
(c)
Interpretation:
To draw the product formed when 1-ethylcyclohex-1-ene reacts with
Concept introduction:
The reaction of alkene with water in presence of acid gives alcohol. First step in the reaction is protonation and formation of carbocation, Second step is addition of nucelophile (water) to the carbocation and then alcohol forms and regeneration of catalyst takes place.
(d)
Interpretation:
To draw the product formed when 1-ethylcyclohex-1-ene reacts with
Concept introduction:
Reaction of alkene with dihalide gives
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General Chemistry: Principles And Modern Applications Plus Mastering Chemistry With Pearson Etext -- Access Card Package (11th Edition)
- (1) Write a complete chemical equation showing reactants, products, and catalysts needed (if any) for the following reaction and (2) Draw and name the organic compound found in every reaction. (a) Complete hydrogenation of 2-Methylhexa-1,5-diene (b) Complete halogenation (Br2) of 3-Ethyl-2,2-dimethylhept-3-ene (c) Reaction of (4E)-2.4-Dimethylhexa-1,4-diene with a mole of water (d) Reaction of cis-3,3-Dimethyl-4-propylocta-1,5-diene with two mole of HBr (e) Reaction of trans-1-Bromo-3-chlorocyclopentane with potassium hydroxide (f) Formation of Gilman reagent using isopropyl bromide (g) Ozonolysis of 3,3-Dimethyloct-4-yne (h) Complete halogenation (Cl2) of 3-Ethyl-5-methyl-1,6,8-decatriyne (i) Partial hydrogenation using Lindlar's Catalyst 2,2,5,5-Tetramethylhex-3-yne (i) Reaction of 3.4-Dimethylcyclodecyne with sodium amidearrow_forwardCompounds A and B are isomers of the molecular formula CyH19Br. Both yield the same alkene Cin an elimination reaction. Hydrogenation of C yields the product 2,3,3,4 tetramethyl pentane. What are the structures of A, B, and C?arrow_forward5B 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_forward
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- Write 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_forward1. (a) Draw structures of the seven isomeric alkynes of formula C6H10 - (b) Give the IUPAC and derived name of each. (c) Indicate which ones will react with Ag' or Cu(NH3)2.arrow_forward(a) Write the IUPAC names of the following compounds :(i) CH3CO(CH2)4CH3 (ii) Ph — CH = CH — CHO(b) Describe the following conversions in not more than two steps :(i) Ethanol to 3-Hydroxybutanal (ii) Benzoic acid to m-Nitrobenzyl alcohol(iii) Propanone to Propenearrow_forward
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