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- Reagent Table Dicyclopentadiene Cyclopentadiene Maleic Anhydride Ethyl Acetate Hexanes cis-norbornene-5,6- endo-dicarboxylic anhydride Melting Point (°C) N/A N/A N/A N/A Boiling Point (°C) N/A N/A Density (g/cm³) Solubility in Water Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Choose... Table view Choose... Choose... ✓ Choose... Liquid Organic Waste Bottle Solid Chemical Waste Bucket Sink with Copious Water Choose... Choose... Choose... Choose... List view Choose... Choose... DisposalWhat is the difference between homolysis vs. heterolysis. Show by giving an example.geraniol OH Reagents a. SOCI₂ b. CH3COCI C. CH₂(CO₂Et)2, CH3CH₂O* Na* d. H3O*, heat e. CH3COCH₂CO₂Et, CH3CH₂O Na* f. CH3CH₂OH geranylacetone Select reagents from the table to carry out this conversion. Enter your answer as a string of letters without spaces or punctuation, i.e. ace.
- Give the appropriate/simplest IUPAC name of the compound (see the attached picture) A.) 5-tert-butyl-2-methylcyclopentanone B.) 2-tert-butyl-5-methylcyclopentanone C.) 2-tertbutyl-5-methylcyclopentanone D.) 2-methyl-5-tertbutylcyclopentanone E.) 5-methyl-2-tertbutylcyclopentanoneConsider the ester functional group shown in the structure below. The reported pK, of methyl acetate is 25. This value is much less than the expected pK, value of 50 for a normal C-H bond. Which of the 3 C-H bonds is responsible for this low pk, value? Explain why methyl acetate has such a low pk, value compared to a normal alkane. H pK, 25this is IR data from acetylsalycilic acid. what are the major diagnostic functional groups shown?...
- a. Would you expect hemiacetals to be stable in basic solutions? Explain your answer.b. Acetal formation must be catalyzed by an acid. Explain why it cannot be catalyzed by CH3O-.c. Can the rate of hydrate formation be increased by hydroxide ion as well as by acid? Explain.Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C. ... NH2 HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one. + 4 n [ ?B\Fill the following blank with appropriate compounds: 1-we can distinguish chemically between aldehyde and ketones by 2-industrial uses for aldehyde and ketones are 3-ethers is good Lewis base because for 4-williamson reaction is most important for synthesis the ..compounds ......... ..compounds. 5-prepare alcohols by hydrolysis for ....compounds .
- Good hand written explanation Asap Thanks What is an azeotrope? a) A mixture of compounds that is dangerous to distill. b) Any mixture that cannot be practically separated by distillation c) A set ratio of compounds that can only be distilled in the best equipment under the best conditions. d) A set ratio of two compounds (e.g. 5% ethanol in water) that always distills together at the same time.4. Which synthesis, starting from benzene, forms aniline (aminobenzene)? a. 1) HNO3/H₂SO4 b. 1) HNO3/H₂SO4 2) H₂, Pd/C c. 1) NH₂/H₂SO4 d. 1) Cl2, FeCl3 2) NaOH, high T,P e. 1) NH₁/H₂SO4 2) H₂, Pd/C1. Construct a chain of 7 carbon atoms that contains an alcohol and an alkyl as a functional group. Name by IUPAC Nomenclature 2. Construct a 9-point cycle that has a carboxylic acid and an ene as functional group. Name by IUPAC Nomenclature 3. construct a carbon chain containing one esters. Name by IUPAC Nomenclature 4. build a chain of 12 carbon atoms that contains as functional group an aldehyde, an aromatic and a cycle. Name by IUPAC Nomenclature