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Arange in ASCENDING orceR each set of opganiC Campuurdus ccorcung to thee rcactiuity tauaras the inctrCaRchon...
Section: 17-14 63. Give the major product for the reaction. Justify your answer. 1. CH, CHECHE...
Section: 17-14 63. Give the major product for the reaction. Justify your answer. 1. CH, CHECHE CH2CH3 CHC осн; 2. HCI excess B) A) C) OO DO DEO CH,CHE CH2CH2 CH:CHE CHCH3 CH, CH2 CHCH CH CH:09 OH CHO D) E) OH =O CH CH3 CH,CHE CHCH CH,CHE CHO O CHO “Η
yea i need 4 5 anx 6 ough the following stepe 20 points) The bromination of...
yea
i need 4 5 anx 6
ough the following stepe 20 points) The bromination of methane proceeds through Br - 2Br CH. Br. CH: Br AN (per mole) E. per mole) 1100 (kral) 100 LJ (45 kcal) C'H + HBr + 73 kJ (17 kcal) 7911 . CH, Br + Br 112 kJ ( 27 kcal) 7 kcal)79 kJ (19 kcal) 27 kcal)4 kJ (1 kcal Draw a complete reaction-energy diagram for this rea b) Label the rate-limiting step....
5. Determine the relationship between each pair in the following set of compounds: same compound, enantiomers...
5. Determine the relationship between each pair in the following set of compounds: same compound, enantiomers or diastereomers. (2 points each) CHs CH CH CHS H CHLCH Br CHS H Br H CH H Br
can you please show the reaction for a couple parts of each question? 3. Draw the...
can you please show the reaction for a couple parts of each
question?
3. Draw the structure(s) of the alkynes formed when the following are reacted with a strong base such as potassium hydroxide or sodium amide. CH ci CH,CHCIK CH3CH2CCHCH BY CH3CCH,CHE CHCH C H3CHCHCH3 CH3CCHE . нус Br Br f. Ci CI (CH3)2CHCHCH2BE (CH3)3CCCHg g. Br h. Ci 4. Draw the structure of the dihalide that could be used to prepare each alkyne shown using a strong base....
Page 6 15. A chain reaction is one that & involves a series of steps b....
Page 6 15. A chain reaction is one that & involves a series of steps b. involves two steps of equal activation energy. e. can be initiated by light d. Involves a series of steps, each of which generates a reactive Intermediate that brings about the next step. e. involves free radicals that have an unusual stability and thereby cause a large quantum yield. involves a series of about the next step.. and thereby 16. The hybridization state of the...
3.30 Are the formulas within each set identical, enantiomers, or diastereomers? and нсін Ay (b) HOH...
3.30 Are the formulas within each set identical, enantiomers, or diastereomers? and нсін Ay (b) HOH CI . Y нон and Но н y НСІ СІ Н (a) A нон нСІ (c) НО Н НО Н and X Сін 3.31 Which of the following are meso compounds? Br Br b) HCH. НО СН, - Br (а) C HT -C C-c Н H7 он CH Br CH,OH Но ОН 1 CH, (e) / VOH (0) HOH (НОН CH,OH н, CHO ОН...
CHEM? 152L QUIZ" 41 Total points 546210(BonusQuestion) is worth3 point1 O 1. What is the IUPAC...
CHEM? 152L QUIZ" 41 Total points 546210(BonusQuestion) is worth3 point1 O 1. What is the IUPAC name of each of the following structures? e pois CH,CHCH,--. CH,CH,CH, CH,CH.CH -H Q 2. Name the functional groups in the following structure: (s points) 3. H3 -CH2CH3 Q 3. How would you differentiate (using a chemical reaction) between the following pair of compounds: (9 points) CH3-CH2CH2-C- CH3 and CH3CH2-C-CH2 CH3 b) CHs CH2 CH3 and c) CHO 0 CH,-CH2C-H and
1 Question 7. (a). Us 7. (a). Using data from Table 6.1, calculate the enthalpy change...
1 Question 7. (a). Us 7. (a). Using data from Table 6.1, calculate the enthalpy change (in kcal/mol) for the following reaction under standard conditions Construct a reaction-energy diagram for this reaction. Make sure you clearly label the parts that represent actants, products, transition state, activation energy and heat of reaction. + HI + HCI OF COMMON BONOS CAMOL TABLE 6.1 BOND DISSOCIATION ENTRIES K/MOL KCAL/MOL Bonds to H H- H H-CH H-CH.CH H-CHICHI H-CICH HỊC-CH-CH, HCC-CH, U/ 185 489...
(10 points) 6. Circle all of the compounds below that are achiral OH сн, н Cl....
(10 points) 6. Circle all of the compounds below that are achiral OH сн, н Cl. OH на C H CI H CI CH снсн, CI H сHсH, Br (10 points) 7. Assign the absolute configuration of the stereooenters in each of the following compounds. NHg CH CHy-CH снон сн, COH H но снсH,B CHs Br HO CHCH Br CHy- он H- снсH
'HNMR - Problem Set-3 How would you distinguish between the compounds in each of the following...
'HNMR - Problem Set-3 How would you distinguish between the compounds in each of the following pairs by 'H NMR? a. CH CH2CH2OCH; and CH3CH2OCH2CH3 b. BrCH CH CH Br and BrCH2CH2CH NO2 CH3 CH3 c. CH:CH-CHCH; and CH3 CH CH CH3 CH CH d. CH3-C-C-OCH; CH OCH and CH3-C-CH; OCH e. H3C CH; -C-CH3 CH; and -CHỤCCH CH 'HNMR-Problem Set-3 (Page 1 of 2) Name Write the structural formula for each of the following compounds from the 'H NMR...
Section: 17-14 63. Give the major product for the reaction. Justify your answer. 1. CH, CHECHE CH2CH3 CHC осн; 2. HCI excess B) A) C) OO DO DEO CH,CHE CH2CH2 CH:CHE CHCH3 CH, CH2 CHCH CH CH:09 OH CHO D) E) OH =O CH CH3 CH,CHE CHCH CH,CHE CHO O CHO “Η
yea
i need 4 5 anx 6
ough the following stepe 20 points) The bromination of methane proceeds through Br - 2Br CH. Br. CH: Br AN (per mole) E. per mole) 1100 (kral) 100 LJ (45 kcal) C'H + HBr + 73 kJ (17 kcal) 7911 . CH, Br + Br 112 kJ ( 27 kcal) 7 kcal)79 kJ (19 kcal) 27 kcal)4 kJ (1 kcal Draw a complete reaction-energy diagram for this rea b) Label the rate-limiting step....
5. Determine the relationship between each pair in the following set of compounds: same compound, enantiomers or diastereomers. (2 points each) CHs CH CH CHS H CHLCH Br CHS H Br H CH H Br
can you please show the reaction for a couple parts of each
question?
3. Draw the structure(s) of the alkynes formed when the following are reacted with a strong base such as potassium hydroxide or sodium amide. CH ci CH,CHCIK CH3CH2CCHCH BY CH3CCH,CHE CHCH C H3CHCHCH3 CH3CCHE . нус Br Br f. Ci CI (CH3)2CHCHCH2BE (CH3)3CCCHg g. Br h. Ci 4. Draw the structure of the dihalide that could be used to prepare each alkyne shown using a strong base....
Page 6 15. A chain reaction is one that & involves a series of steps b. involves two steps of equal activation energy. e. can be initiated by light d. Involves a series of steps, each of which generates a reactive Intermediate that brings about the next step. e. involves free radicals that have an unusual stability and thereby cause a large quantum yield. involves a series of about the next step.. and thereby 16. The hybridization state of the...
3.30 Are the formulas within each set identical, enantiomers, or diastereomers? and нсін Ay (b) HOH CI . Y нон and Но н y НСІ СІ Н (a) A нон нСІ (c) НО Н НО Н and X Сін 3.31 Which of the following are meso compounds? Br Br b) HCH. НО СН, - Br (а) C HT -C C-c Н H7 он CH Br CH,OH Но ОН 1 CH, (e) / VOH (0) HOH (НОН CH,OH н, CHO ОН...
CHEM? 152L QUIZ" 41 Total points 546210(BonusQuestion) is worth3 point1 O 1. What is the IUPAC name of each of the following structures? e pois CH,CHCH,--. CH,CH,CH, CH,CH.CH -H Q 2. Name the functional groups in the following structure: (s points) 3. H3 -CH2CH3 Q 3. How would you differentiate (using a chemical reaction) between the following pair of compounds: (9 points) CH3-CH2CH2-C- CH3 and CH3CH2-C-CH2 CH3 b) CHs CH2 CH3 and c) CHO 0 CH,-CH2C-H and
1 Question 7. (a). Us 7. (a). Using data from Table 6.1, calculate the enthalpy change (in kcal/mol) for the following reaction under standard conditions Construct a reaction-energy diagram for this reaction. Make sure you clearly label the parts that represent actants, products, transition state, activation energy and heat of reaction. + HI + HCI OF COMMON BONOS CAMOL TABLE 6.1 BOND DISSOCIATION ENTRIES K/MOL KCAL/MOL Bonds to H H- H H-CH H-CH.CH H-CHICHI H-CICH HỊC-CH-CH, HCC-CH, U/ 185 489...
(10 points) 6. Circle all of the compounds below that are achiral OH сн, н Cl. OH на C H CI H CI CH снсн, CI H сHсH, Br (10 points) 7. Assign the absolute configuration of the stereooenters in each of the following compounds. NHg CH CHy-CH снон сн, COH H но снсH,B CHs Br HO CHCH Br CHy- он H- снсH
'HNMR - Problem Set-3 How would you distinguish between the compounds in each of the following pairs by 'H NMR? a. CH CH2CH2OCH; and CH3CH2OCH2CH3 b. BrCH CH CH Br and BrCH2CH2CH NO2 CH3 CH3 c. CH:CH-CHCH; and CH3 CH CH CH3 CH CH d. CH3-C-C-OCH; CH OCH and CH3-C-CH; OCH e. H3C CH; -C-CH3 CH; and -CHỤCCH CH 'HNMR-Problem Set-3 (Page 1 of 2) Name Write the structural formula for each of the following compounds from the 'H NMR...
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