1. A compound has molecular formula of C8H8O and every mole of this compound is able...
1. A compound has molecular formula of C8H8O and every mole of
this compound is able to react with 4 moles of H2 in a complete
catalytic hydrogenation. How many ring(s) is/are there in this
compound? ___ How many pi bond(s) is/are there in this compound?
____
2. A compound has molecular formula of C6H8O and every mole of this
compound is able to react with 1 mole of H2 in a complete catalytic
hydrogenation. How many ring(s) is/are there in this compound? ___
How many pi bond(s) is/are there in this compound? ____
Can someone please explain how to do these two.. very confused, just need a bit of help! thank you, bless :)
Homework Answers
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1. A compound has molecular formula of C8H8O and every mole of
this compound is able...
please explain 4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar...
please explain
4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data
4. An unknown hydrocarbon has...
Squalene, an important intermediate in the biosynthesis of steroids, has the molecular formula C30H50 and has...
Squalene, an important intermediate in the biosynthesis of steroids, has the molecular formula C30H50 and has no triple bonds. (a) What is the index of hydrogen deficiency of squalene? (b) Squalene undergoes catalytic hydrogenation to yield a compound with the molecular formula C30H62. How many double bonds does a molecule of squalene have? (c) How many rings?
Compound a has the formula C10H16
Compound a has the formula C10H16. on catalytic hydrogenation on Pd, it reacts with 1 molar equivalent of H2. Compound A also participates in the reaction with ozone, and then treated with Zn/H3O+ to obtain a symmetric diketon B, C10H16O2. a) How many rings does compound A contain? b) the structure of a and b c) write down the reactions that take place
Compound, C, has the molecular formula C7H 12. On catalytic hydrogenation, 1 mol of C absorbs...
Compound, C, has the molecular formula C7H 12. On catalytic hydrogenation, 1 mol of C absorbs 1 mol of hydrogen and yields a compound with the molecular formula C 7H 14. On ozonolysis and subsequent hydrolysis, C yields only: 0 CH?CCHCHCHCHCH The structure ofCis CH CH, Hj IV
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14....
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14. Upon catalytic hydrogenation over Pa/C it reacts with only one equivalent of hydrogen. Suggest a possible structure for Compound A. (There are MANY possible correct answers here.) Praw all of the dehydration products that are formed from the following compound.
17) A compound has an empirical formula of C3H11O3. If its molecular formula is 238 g/mole,...
17) A compound has an empirical formula of C3H11O3. If its molecular formula is 238 g/mole, what is its molecular formula?
Compound F has a molecular formula of C9H8O. What is the unsaturation number; Functional groups that...
Compound F has a molecular formula of C9H8O. What is the
unsaturation number; Functional groups that are ppossibly present
in compound F?
I keep getting this question wrong, can anyone help me?
7 of 29 Incorrect Question 27 of Map Compound F has a molecular formula of CgHgO. What is the Unsaturation Number (UN) or Double-Bond Equivalent (DBE)? Number Examine the IR spectrum provided for Compound F Based on the molecular formula, the UN/DBE you calculated, and the IR spectrum,...
30) 30) A compound X of molecular formula CgH12 with no triple bonds reacts with one...
30) 30) A compound X of molecular formula CgH12 with no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula CgH14. What can be inferred about the structure of compound X? A) Compound X has 2 rings and 1 p bond. B) Compound X has 3 p bonds. C) Compound X has 1 ring and 2 p bonds. D) Compound X has 3 rings. 31) Determine the product of the following reaction. Н....
what is the molecular formula of the structure? how many sigma bonds are present in the...
what is the molecular formula of the structure?
how many sigma bonds are present in the steucture as
drawn?
how many pi bonds are present in the structure as draw?
what is the hybridization of every carbon in the left most
ring
IN
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2...
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2 are upon catalytic hydrogenation. When Compound A is treated with KMnO4 the following compounds form. What is the structure of A? O C-OH + HO-C-CH,CHCH2-C-OH CH3 -C-OH 3° unsat 3 the equiv
please explain
4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data
4. An unknown hydrocarbon has...
Compound, C, has the molecular formula C7H 12. On catalytic hydrogenation, 1 mol of C absorbs 1 mol of hydrogen and yields a compound with the molecular formula C 7H 14. On ozonolysis and subsequent hydrolysis, C yields only: 0 CH?CCHCHCHCHCH The structure ofCis CH CH, Hj IV
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14. Upon catalytic hydrogenation over Pa/C it reacts with only one equivalent of hydrogen. Suggest a possible structure for Compound A. (There are MANY possible correct answers here.) Praw all of the dehydration products that are formed from the following compound.
17) A compound has an empirical formula of C3H11O3. If its molecular formula is 238 g/mole, what is its molecular formula?
Compound F has a molecular formula of C9H8O. What is the
unsaturation number; Functional groups that are ppossibly present
in compound F?
I keep getting this question wrong, can anyone help me?
7 of 29 Incorrect Question 27 of Map Compound F has a molecular formula of CgHgO. What is the Unsaturation Number (UN) or Double-Bond Equivalent (DBE)? Number Examine the IR spectrum provided for Compound F Based on the molecular formula, the UN/DBE you calculated, and the IR spectrum,...
30) 30) A compound X of molecular formula CgH12 with no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula CgH14. What can be inferred about the structure of compound X? A) Compound X has 2 rings and 1 p bond. B) Compound X has 3 p bonds. C) Compound X has 1 ring and 2 p bonds. D) Compound X has 3 rings. 31) Determine the product of the following reaction. Н....
what is the molecular formula of the structure?
how many sigma bonds are present in the steucture as
drawn?
how many pi bonds are present in the structure as draw?
what is the hybridization of every carbon in the left most
ring
IN
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2 are upon catalytic hydrogenation. When Compound A is treated with KMnO4 the following compounds form. What is the structure of A? O C-OH + HO-C-CH,CHCH2-C-OH CH3 -C-OH 3° unsat 3 the equiv
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