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Vanillin is the common name for 4-hydroxy-3-methoxy-benzaldehyde.
See attached figure for the structure.
Vanillin have 3 functional groups:
1) aldehyde group: R-HC=O, in which the carbon is double bonded to oxygen
2) phenolic hydroxide group: R-OH, were the hydroxyl group is bounded to a carbon from the benzene ring
3) ether group: R-O-R, were hydrogen is bounded through sigma bonds to carbons
Now for the hybridization we have:
The carbon atoms involved in the benzene ring and the red carbon atom (from the aldehyde group) have a <u>sp²</u> hybridization because they are involved in double bonds.
The carbon atom from the methoxy group (R-O-CH₃) and the blue oxygen's have a <u>sp³</u> hybridization because they are involved only in single bonds.
Answer:
59.30% I
Explanation:
mi respuesta es esa porque es la más sercana
Answer:
FALSE
Since 0.385 < 0.526, the value for week 3 is accepted.
Explanation:
Qexp = (|Xq - Xₙ₋₁|)/w
where Xq is the suspected outlier; Xₙ₋₁ is the next nearest data point; w is the range of data
First, the data are arranged in decreasing order, from highest to lowest:
3. 5.6
2. 5.1
8. 5.1
1. 4.9
6. 4.9
5. 4.7
7. 4.5
4. 4.3
Xq = 5.6; Xₙ₋₁ = 5.1; w = 5.6 - 4.3 = 1.3
Qexp = (|5.6 - 5.1|)/1.3 = 0.385
From tables, at 95% confidence level, for n = 8, Qcrit = 0.526
Since 0.385 < 0.526, the value for week 3 is accepted.