Answer:
C
Explanation: a is incorrect since the lower the ph = more acidic and b is incorrect because it produces hydronium ion and d I’m not sure what it is but I no that base recieve the protons
Answer:
d.
Explanation:
i was think b at first but that doesnt really explain how it gets to the circulatory system so d because without the the regulation of the heart rate and oxgen rich blood the muscular system can do absolutely nothing
The product for the following reaction are :
- 2 - butanone
- CH₃CH₂COCl
- CH₃CH₂CONHCH₃
T carboxylic acid is an organic compound. the functional group of carboxylic acid is carboxy. general formula is given as : R - COO⁻.
The reactions are given as follows :
1) the reduction of carboxylic acid into ketone with the organometallic compound is given as follows :
CH₃CH₂COOH + CH₃Li ------> CH₃CH₂COCH₃
2 butanone
2) the reaction of carboxylic acid with SOCl₂ is given as follows :
CH₃CH₂COOH + SOCl₂ -----> CH₃CH₂COCl
3) the reaction of carboxylic acid with CH₃NH₂ is given as follows
CH₃CH₂COOH + CH₃NH₂ -----> CH₃CH₂CONHCH₃
Thus, The product for the following reaction are :
- 2 - butanone
- CH₃CH₂COCl
- CH₃CH₂CONHCH₃
To learn more about carboxylic acid here
brainly.com/question/4721247
#SPJ4
Answer:
See explanation and images attached
Explanation:
We know that the cis isomer has more heat of hydrogenation since it is less stable than the trans isomer. Since the hydrogenation of both compounds yields the same product and the hydroboration/oxidation both give a primary alcohol, they are geometric isomers and Y is the trans isomer (Image 2).
For the compound C8H12, the compound in question must be 1,5- cyclooctadiene since two moles of the same aldehyde was obtained after ozonolysis and reaction with two equivalents of hydrogen gives cyclooctane (Image 1).
Answer:
It will go faster each time because she is stirring therefore the water can get to the salt faster than it just sitting at the top
Explanation:
