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- Q2) Prepare Y from X each of the following (Thirteen only) :- X Y 1 hex-2-ene 2-chlorohexan-3-ol Propan 2-one 2 prop-1-yne 3 benzene styrene 4 phenylmethanol Benzoic acid 5 Trans-penta 2-ene Penta 2-yne Benzene 6 Durene 7 1-bromo cyclo pentan cyclo pentan 8 Methyl cyclohexane Toluene 9 Benzene m-bromo nitro benzene 10 ethylene Ethylene glycol 11 Tert-butyl chlorid 2,2dimethyl hexane 12 2-3dibromo butane 2-butene 13 Toluene p-nitro benzoic acid 14 Sec-butyl bromide butane 15 benzene m-nitro benzoic acidName the following organic compound: CH3 S CH CH3 CH 0 CH, CH, 3-methylsulfide-2-ethoxy butane 2-ethoxy-3-methylthio butane O 3-ethoxy-2-methylthio butane O 2-methylsulfide-3-ethoxy butane O 2-ethoxy-3-methylsulfide butaneDraw a structural formula for the major organic product of the reaction shown below. & CH₂ (oran CH3CH₂O -CuLi 2 ether You do not have to consider stereochemistry. Sn [F ? ChemDoodle H3O +
- Provide an appropriate name for the following compound. 3-fluro u-methyl 5-chloro 7 OH CI F 5-chbro-3 fluro-4 methyl non-2-enol 2) Draw the molecule that corresponds to (3R,5R,6R)-5-cyclopropyl-6-ethyl-3-iodo-1-methylcyclohex-1-ene.JF-M05 What is the product of the following reaction? H;C-CH2-CH=CH2 HBr + JF-MO5 H,C-CH-CH,-CH3 Br JF-MO5а H3C-CH2-CH2-CH2 Br JF-MO56 H3C-CH2-CH-CH2 Br Br JF-MO5c H3C-CH-CH-CH3 Br Br JF-M05dnent/takeCovalentActivity.do?16cal assigi [Review Topics] [References] Use the References to access important values if needed for this question. Draw a structural formula for the major organic anion formed when 2- ethylbutanal is reacted with Tollens' reagent. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. P. opy aste CH4 ChemDoodle Previous Nex
- 1-Ethoxypropane is: O CH3CH₂OCH₂CH³ Ⓒ CH³CHCH₂OCH3 O CH3CH₂CH₂CH₂CH3 O CH3CH₂CH2CH2CH₂CH3 OCH3CH₂CH₂CH₂OCH32 Write the IUPAC name for each compound. Ο COC-M (a) HV Ο 0 || (d) H₂N- C (b) CH₂(CH₂),COCH, OTT HO noitos2) alodo d diw sobirbydaA to noilo ono evig of alcools dikw 39891 abitbydA (8.81 (c) CH₂(CH₂)4CNHCH, no bae totes me to slom 0 O CNH₂ با нио но но но HOOH + HOOO HO HOOOH OHO.HOOD HO || (e) CH₂CO-A iw sobixbydnA to noltoso. driw do A (D681 moitoo@) aoniMA "I w bn shomme a onions to solomeowths of elom ono bas shima Joubo aviy oj vig OH OHO bertiup bios biydisororesidenten (f) CH3CHCH₂COCH₂CH3Draw the structure of the products formed in the following reactions. a) CN H,0, H* CH3 он b) H3C- -CI + CH3 c) CH3 KMNO4, A, H,O" CH3 d) Br Mg, éther CO, H*
- (a) Rank the following carbocations in order of increasing electrophilicity (1 = lowest electrophilicity, 4 = highest electrophilicity). (b) Rank the following 1,1-halomethylcyclopentanes in order of reactivity in an SN1 reaction (1 = lowest reactivity, 4 = highest reactivity. CH3 CI B with SNI, nor reactive means more stable (c) Rank the following species in terms of increasing nucleophilicity in an SN2 reaction in a po aprotic solvent (1 = lowest nucleophilicity, 4 = highest nucleophilicity).1-Chloro-4-isopropylcyclohexane exists as two stereoisomers: one cis and one trans. Treatment of either isomer with sodium ethoxide in ethanol gives 4-isopropylcyclohexene by an E2 reaction. CH,CH,O Na* CI CH,CH,OH 1-Chloro-4- 4-Isopropylcyclohexene isopropylcyclohexane The cis isomer undergoes E2 reaction several orders of magnitude faster than the trans isomer. How do you account for this experimental observation?Kelerences Keview topic Draw a structural formula for the major product of the reaction shown. Cl2 H20 CH;CH2CH;CH=CHz • Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. Do not show stereochemistry in other cases. • If the reaction produces a racemic mixture, just draw one stereoisomer. 2reg 2reg M) ots 2reg pts 2req 1 pts 2req 1 pts 2reg ...1 pts ChemDoodle Previous Next> Save and Exit APR tv MacBook Air 80 DII DD F3 F4 FS F6 F7 F8 F10 F1 F12 #3 $ & + 3 4 6. 7 8 %3D dele E Y | { } P [ F G H. J K C V N M ? .. .. * C0 B