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please solve this organic chem question thank you Naprer (8) 5. Prepare the following compounds using...
please solve this organic chem question thank you BHA VUN V chapter (8) 5. Prepare the...
please solve this organic chem question thank you
BHA VUN V chapter (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. - ( a) CHANH, synthesis NH3 D) CH, CH CHE 0-CH, CH, Sh2 ether Synthesis
please solve this organic chem question thank you BHA VUN V chapter (8) 5. Prepare the...
please solve this organic chem question thank you
BHA VUN V chapter (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. - ( a) CHANH, synthesis NH3 D) CH, CH CHE 0-CH, CH, Sh2 ether Synthesis
Please show steps and explain (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations....
Please show steps and explain
(8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. a) CH NH2 b) CH, CHCH 0-CH, CH
orgo chem help?? need help on a thank you 0 OCH o) CH2-CCHE HO OCHCHH CH...
orgo chem help??
need help on a thank you
0 OCH o) CH2-CCHE HO OCHCHH CH HOOAC)/ WU Nabi chapter (8) 5. Prepare the following compounds usi with alkyl-halides, alcohols, thiols, cte (4) CH,NH, etc., and nucleophilic substitution and eliminations. Start organics. Any common solvent is allowed. synthesis NH3 DJ CH₃ CH CH₂ 0-CHCH, 842 ether Synthesis
whats the answer to these reactions? please help Name Jigsa OCH, CH, - сня n) CH2-CCH•...
whats the answer to these reactions? please help
Name Jigsa OCH, CH, - сня n) CH2-CCH• 0 CH3 o) CH, CCH HOCH, CH, BH, THF H.O.OH Hg(OAc), /HO NaBH (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. a) CH, NH2 b) CH CH CHE 0-CH, CH
PLEASE HELP WITH THESE. THANK YOU How are the following two compounds related? CH CH3 HO...
PLEASE HELP WITH THESE. THANK
YOU
How are the following two compounds related? CH CH3 HO -H HO -Н Given the following substitution reaction, what would the effect be of changing the solvent from CH3OH to (CH3)2S=0? H- OH H OH VS HO -H H -OH H -OH HO H + CH (CH2CH2-Br NaOH CH;(CH2), CH2-OH + NaBr CH OH CH2OH A. The reaction rate will increase. OB. There is no effect on the rate of the reaction, C. The...
4.) Name the following compounds All please!! Thank you in advance f. CH2CH3 CH2CH=CHCHCH CH2-CH 8....
4.) Name the following compounds
All please!! Thank you in advance
f. CH2CH3 CH2CH=CHCHCH CH2-CH 8. CH-CH2-CH-CH-C-CH-CH, CH2-CHE h. CH,CH CH CH CH CH CHCHCH_CH, ts i. CH CH.CH.CH.CECCH. CH2-CH CH3 -CH-CH2-CH-CH2-CH-CH,
1) State which of the electrophiles given below will react preferentially by i) SN1, ii) by...
1) State which of the electrophiles given below will react
preferentially by i) SN1, ii) by SN2, or iii) capable of reacting
by either of the two mechanisms depending on the given conditions.
How can you affect those conditions to favour SN1 or SN2? Reason
your predictions based on the structures of the compounds. Br-CH3,
Br-CH2CH3, Br-CH(CH3)2, Br-C(CH3)3, Br-CH2-C5H6; C5H6 = phenyl
Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via...
Organic Chemistry please help asap 70. What nucleophiles wou cleophiles would form the following compounds as...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
PLEASE ANSWER ALL PARTS OF THE QUESTION CORRECTLY. THANK YOU FOR YOUR HELP! Q1. The following...
PLEASE ANSWER ALL PARTS OF THE QUESTION CORRECTLY.
THANK YOU FOR YOUR HELP!
Q1. The following compounds are drugs that have been developed or tested to treat cancer. A) Circle and identify the functional groups found in each structure, B) indicate type of interactions (intermolecular forces) would occur for each compound in water versus octanol (chemical formula CH(CH2),OH). C) indicate which solvent would best dissolve the compound water or octanol and why you chose the answer you did. Compound 1:...
please solve this organic chem question thank you
BHA VUN V chapter (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. - ( a) CHANH, synthesis NH3 D) CH, CH CHE 0-CH, CH, Sh2 ether Synthesis
please solve this organic chem question thank you
BHA VUN V chapter (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. - ( a) CHANH, synthesis NH3 D) CH, CH CHE 0-CH, CH, Sh2 ether Synthesis
Please show steps and explain
(8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. a) CH NH2 b) CH, CHCH 0-CH, CH
orgo chem help??
need help on a thank you
0 OCH o) CH2-CCHE HO OCHCHH CH HOOAC)/ WU Nabi chapter (8) 5. Prepare the following compounds usi with alkyl-halides, alcohols, thiols, cte (4) CH,NH, etc., and nucleophilic substitution and eliminations. Start organics. Any common solvent is allowed. synthesis NH3 DJ CH₃ CH CH₂ 0-CHCH, 842 ether Synthesis
whats the answer to these reactions? please help
Name Jigsa OCH, CH, - сня n) CH2-CCH• 0 CH3 o) CH, CCH HOCH, CH, BH, THF H.O.OH Hg(OAc), /HO NaBH (8) 5. Prepare the following compounds using nucleophilic substitution and eliminations. Start with alkyl halides, alcohols, thiols, etc., and inorganics. Any common solvent is allowed. a) CH, NH2 b) CH CH CHE 0-CH, CH
PLEASE HELP WITH THESE. THANK
YOU
How are the following two compounds related? CH CH3 HO -H HO -Н Given the following substitution reaction, what would the effect be of changing the solvent from CH3OH to (CH3)2S=0? H- OH H OH VS HO -H H -OH H -OH HO H + CH (CH2CH2-Br NaOH CH;(CH2), CH2-OH + NaBr CH OH CH2OH A. The reaction rate will increase. OB. There is no effect on the rate of the reaction, C. The...
4.) Name the following compounds
All please!! Thank you in advance
f. CH2CH3 CH2CH=CHCHCH CH2-CH 8. CH-CH2-CH-CH-C-CH-CH, CH2-CHE h. CH,CH CH CH CH CH CHCHCH_CH, ts i. CH CH.CH.CH.CECCH. CH2-CH CH3 -CH-CH2-CH-CH2-CH-CH,
1) State which of the electrophiles given below will react
preferentially by i) SN1, ii) by SN2, or iii) capable of reacting
by either of the two mechanisms depending on the given conditions.
How can you affect those conditions to favour SN1 or SN2? Reason
your predictions based on the structures of the compounds. Br-CH3,
Br-CH2CH3, Br-CH(CH3)2, Br-C(CH3)3, Br-CH2-C5H6; C5H6 = phenyl
Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCI, HBr, or HI) via...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
PLEASE ANSWER ALL PARTS OF THE QUESTION CORRECTLY.
THANK YOU FOR YOUR HELP!
Q1. The following compounds are drugs that have been developed or tested to treat cancer. A) Circle and identify the functional groups found in each structure, B) indicate type of interactions (intermolecular forces) would occur for each compound in water versus octanol (chemical formula CH(CH2),OH). C) indicate which solvent would best dissolve the compound water or octanol and why you chose the answer you did. Compound 1:...
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