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Chemistry 11

Tuesday, May 24, 2011. Purpose: To synthesize an ester from a carboxylic acid and an alcohol. Observation: We created methyl salicylate which had a faint but noticeable minty smell. Problems that could have occurred to not create a strong scent could be that we did not put in the correct amounts of salicylic acid, methanol, and/or sulphuric acid. Not giving it enough time or too much time boiling and cooling could also affect the synthesizing of our ester. Monday, May 23, 2011. Saturday, May 14, 2011.

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Chemistry 11 | mmthkpjds.blogspot.com Reviews

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Tuesday, May 24, 2011. Purpose: To synthesize an ester from a carboxylic acid and an alcohol. Observation: We created methyl salicylate which had a faint but noticeable minty smell. Problems that could have occurred to not create a strong scent could be that we did not put in the correct amounts of salicylic acid, methanol, and/or sulphuric acid. Not giving it enough time or too much time boiling and cooling could also affect the synthesizing of our ester. Monday, May 23, 2011. Saturday, May 14, 2011.

<META> KEYWORDS

1 chemistry 11

2 esterfication lab

3 materials isopropyl alcohol

4 methanol

5 salicylic acid

6 octyl alcohol

7 formic acid

8 acetic acid

9 concentrated sulphuric acid

10 water

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chemistry 11,esterfication lab,materials isopropyl alcohol,methanol,salicylic acid,octyl alcohol,formic acid,acetic acid,concentrated sulphuric acid,water,eye droppers,test tubes,posted by,no comments,email this,blogthis,share to twitter,share to facebook

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Chemistry 11 | mmthkpjds.blogspot.com Reviews

https://mmthkpjds.blogspot.com

Tuesday, May 24, 2011. Purpose: To synthesize an ester from a carboxylic acid and an alcohol. Observation: We created methyl salicylate which had a faint but noticeable minty smell. Problems that could have occurred to not create a strong scent could be that we did not put in the correct amounts of salicylic acid, methanol, and/or sulphuric acid. Not giving it enough time or too much time boiling and cooling could also affect the synthesizing of our ester. Monday, May 23, 2011. Saturday, May 14, 2011.

INTERNAL PAGES

mmthkpjds.blogspot.com

1

Chemistry 11: January 2011

http://mmthkpjds.blogspot.com/2011_01_01_archive.html

Saturday, January 22, 2011. Mole to Mole Conversions. Coefficients in balanced equations tell us the number of moles reacted or produced. They can also be used as conversion factors. WHAT YOU NEED OVER WHAT YOU HAVE. Coefficients have to be in moles. 6 mol B x 1A (what we need)= 2 mol of A. 3B (what we have). 025 mol of A x 3.5 B = 0.88 mol. Thursday, January 20, 2011. Stoichiometry is a branch of chemistry that deals with the quantitative analysis of chemical reactions. 6 types of Reactions. Empirical f...

2

Chemistry 11: Esterfication Lab

http://mmthkpjds.blogspot.com/2011/05/esterfication-lab.html

Tuesday, May 24, 2011. Purpose: To synthesize an ester from a carboxylic acid and an alcohol. Observation: We created methyl salicylate which had a faint but noticeable minty smell. Problems that could have occurred to not create a strong scent could be that we did not put in the correct amounts of salicylic acid, methanol, and/or sulphuric acid. Not giving it enough time or too much time boiling and cooling could also affect the synthesizing of our ester. Subscribe to: Post Comments (Atom).

3

Chemistry 11: Functional Groups Alcohols Halides

http://mmthkpjds.blogspot.com/2011/05/functional-groups-alcohols-halides.html

Monday, May 2, 2011. Functional Groups Alcohols Halides. Organic compounds can contain elements other than C and H. These are known as functional groups. Carbon chains without functional groups are written as -R. An alcohol is a hydrocarbon with a -OH bonded to it. Same naming rules apply but the parent chain ends with and -ol. If a compound has more than one -OH group number add -diol,triol, etc endings. Group 7 elements (F,Cl,Br,I) can bond to a hydrocarbon chain. Subscribe to: Post Comments (Atom).

4

Chemistry 11: May 2011

http://mmthkpjds.blogspot.com/2011_05_01_archive.html

Tuesday, May 24, 2011. Purpose: To synthesize an ester from a carboxylic acid and an alcohol. Observation: We created methyl salicylate which had a faint but noticeable minty smell. Problems that could have occurred to not create a strong scent could be that we did not put in the correct amounts of salicylic acid, methanol, and/or sulphuric acid. Not giving it enough time or too much time boiling and cooling could also affect the synthesizing of our ester. Monday, May 23, 2011. Saturday, May 14, 2011.

5

Chemistry 11: More Functional Groups

http://mmthkpjds.blogspot.com/2011/05/more-functional-groups.html

Monday, May 2, 2011. Carboxylic acids are formed by the function group (The "R" means it's a chain). Use standard rules but change the parent changing ending to -oic acid. The simplest carboxylic acid is methanoic acid. 3 Chloro, 3 methyl, butanoic acid. An Ether contains an oxyegen group connected to two alkyl (carbon) chains. Name the small alkyl group first, then the second alkyl group followed by the Ether. Subscribe to: Post Comments (Atom). More Functional Groups: Carboxylic acids, Ethers, .

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mmthkpjds.blogspot.com

Chemistry 11

Tuesday, May 24, 2011. Purpose: To synthesize an ester from a carboxylic acid and an alcohol. Observation: We created methyl salicylate which had a faint but noticeable minty smell. Problems that could have occurred to not create a strong scent could be that we did not put in the correct amounts of salicylic acid, methanol, and/or sulphuric acid. Not giving it enough time or too much time boiling and cooling could also affect the synthesizing of our ester. Monday, May 23, 2011. Saturday, May 14, 2011.

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