7. When the compound below is subjected to dehydration conditions, the expected alkene is notformed. Explain why. (Hint: Try making a model of the product.).HO.ASOMFTHFnot formed

The geometry should be planar to form an alkene the bridge head position in alkene is sp2…

Answered: 7. When the compound below is subjected…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 3CTQ

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Please explain.
7. Fill in the missing information.
What major alkene product is produced by dehydrating the following alcohols?a. Cyclohexanolb. 1-Methylcyclohexanolc. 2-Methylcyclohexanold. 2,2-Dimethylcyclohexanole. 1,2-Cyclohexanediol (Hint: Consider keto–enol tautomerism.)
Please see image below. #5 only.
Draw the structure for an alkene that gives the following reaction product. CH3 HCI CH3CHCH2CHCH3 CI • Ignore alkene stereochemistry. •You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. P. opy aste ChemDoodle"
Subject: chemistry
1a and 1d
Draw the organic products formed in each reaction. H,N. a. CH;OH, H* OH (CH3),CO. е. H2 OCH,C3H5 Pd-C H CH(CH3)2 H CH(CHa)2 H2N b. CeHsCH,OH, H* HBr но. f. starting material in (e) CH,COOH H CH,CH(CH3)2 [(CH3),COCOLO (CH3CH2);N CF;COOH с. NH,CH2COOH g. product in (e) DCC OH NazCO3 d. product in (b) + product in (c) Fmoc-CI H,N H H20
3. ( Predict the organic product(s) of the reaction of 2-butene with each reagent. a. H₂O (H₂SO4) b. Cl₂ c. Br₂ in H₂O
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Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. Ⓒ. CCl₂ • You do not have to consider stereochemistry. . Include all valence lone pairs in your answer. . In cases where there is more than one answer, just draw one. Bo H₂SO4 First stage in synthesis of the insecticide DDT, which is now banned in the US #₂ SAIF CI OH CC13
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7. When the compound below is subjected to dehydration conditions, the expected alkene is not formed. Explain why. (Hint: Try making a model of the product.) .HO. ASO MF THF not formed