Draw three isomers for a chloro alkane having 4 carbons and identify them as primary, secondary and tertiary alkyl halides. Explain SN2 mechanism for the reaction of one of the isomer with KOH marks) (5.0 Maximum size for new files: 80MB Files 3. 3. You can drag and drop files here to add them. Accepted file types All file types Next page MacBook Air

Draw three isomers for a chloro alkane having 4 carbons and identify them as primary, secondary and tertiary alkyl halides. Explain SN2 mechanism for the reaction of one of the isomer with KOH marks) (5.0 Maximum size for new files: 80MB Files 3. 3. You can drag and drop files here to add them. Accepted file types All file types Next page MacBook Air

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

ChapterL2: Mass Spectrometry

Section: Chapter Questions

Problem 20CTQ

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drop down for the first selection is NH4Cl and CH3COOH and the second drop down is NH3 and NaCH3COOH
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(d0 9 with explanation )
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Two successive reactions, A→B and B→C, haveyields of 73% and 68%, respectively. What is the overall percentyield for conversion of A to C?
Provided the following information determine Δ?ΔHformation of C2H6(g). C(graphite) + O2(g) ⟶⟶ CO2(g) Δ?=−393.5??ΔH=−393.5kJ H2(g) + 1212O2(g) ⟶⟶ H2O(l) Δ?=−285.8??ΔH=−285.8kJ C2H6(g) + 7272O2(g) ⟶⟶ 2CO2(g) + 3H2O(l) Δ?=−1560.7??
plz dont copy ansewrs from other sources and make it your own (there are conflicting answers in other sources)
( is the answer is + 46.48 or -46.48 plzz telll ...why + or why - also explain
Organic Chemistry 1 Absolute Configuration S or R (CIP) Explain all of the steps clearly and logically. Do not just draw a picture. Clearly explain your answer in a step-by-step fashion. Here is the instructor's solution (answer/explanation) to the problem. Please read the professor's solution carefully and explain it here. I have the solutions since the assignment has been turned in. I want to understand why the answer key is correct, and I need a more detailed explanation than the answer key.
How did you convert the c to k that's my only question like 25.5c to k and you got 298.65?
D-Xylose in aqueous solution exists in the pyranose form as a mixture of α and β anomers. Furanose and acyclic forms are present in negligible amounts and can be ignored. A sample of pure α-D-xylopyranose is dissolved in pure neutral water. The optical rotation is then measured immediately using a polarimeter. The specific rotation [??]?? is +93.6°. The optical rotation is then observed to decrease with the passage of time, and the solution is allowed to reach equilibrium. Eventually the specific rotation stabilises at [??]?? = +18.8°. The anomeric ratio at equilibrium a : β is 37 : 63. A sample of pure β-D-xylopyranose is not available. Using this information, predict the specific rotation of pure β-D-xylopyranose. Show how the a and β anomers equilibrate using a mechanism, assuming the presence of a trace amount of base as catalyst.