Introductory Organic and Biochemistry
179 videos • 21,179 views • by Roxi Hulet
1
1: Drawing condensed structures
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2
2: Drawing and reading line structures
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3
3: ldentifying functional groups
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4
4: Predicting the solubility of organic molecules
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5
4a: Identifying functional groups, predicting solubility, and counting carbon
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6
5: Alkanes
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7
6: Constitutional isomers
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8
7: Naming unbranched alkanes
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9
8: Naming alkanes with branches
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10
9: Naming alkanes with halogens
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11
10: Naming cycloalkanes with branches or halogens
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12
10a: Naming alkanes
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13
11: Naming alkenes
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14
12: Naming alkynes
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15
12a: Naming alkenes and alkynes
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16
13: Identifying cis and trans isomers
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17
13a: Classifying alkenes as cis or trans
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18
14: Oral contraceptives
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19
15: Hydrogenation and halogenation of alkenes
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20
16: Hydrohalogenation and Markovnikov’s Rule
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21
17: Hydration of an alkene
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22
17a: Reactions of alkenes
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23
18: Introduction to aromatic compounds
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24
19: Naming alcohols
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25
19a: Naming alcohols
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26
20: Dehydration of alcohols and Zaitsev’s Rule
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27
21: Oxidation of alcohols
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28
22: Metabolism of ethanol
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29
23: Ethers as general anesthetics
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30
24: Constitutional isomers vs. stereoisomers
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31
25: Chirality and enantiomers
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32
26: Chirality centers
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33
26a: Chirality centers and enantiomers
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34
27: Chiral pharmaceuticals
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35
28: Fischer projections
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36
28a: Fischer projections
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37
29: Naming aldehydes and ketones
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38
29a: Naming aldehydes and ketones
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39
30: Interesting aldehydes and ketones
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40
31: Oxidation of aldehydes
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41
32: Reduction of aldehydes and ketones
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42
32a: Reduction of aldehydes and ketones
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43
33: Acetals and hemiacetals
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44
33a: Acetals and hemiacetals
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45
34: Converting acetals to ketones or aldehydes
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46
35: Naming carboxylic acids
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47
36: Naming esters
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48
36a: Naming carboxylic acids and esters
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49
37: Interesting carboxylic acids, esters, and amides
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50
38: Acidity of carboxylic acids
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51
39: Aspirin
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52
40: Converting carboxylic acids to esters
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53
41: Hydrolysis of esters
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54
42: Saponification
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55
43: Intro to amines and amides
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56
43a: Classifying amines
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57
44: Alkaloids
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58
45: Amines as bases
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59
45a: Amines as bases
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60
46: Neurotransmitters
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61
47: Epinephrine and histamine
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62
48: Hormones vs. neurotransmitters
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63
49: Introduction to lipids
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64
50: Introduction to fatty acids
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65
50a: Drawing the structures of fatty acids
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66
51: Introduction to waxes
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67
52: Triacylglycerols
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68
52a: Drawing triacylglycerols
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69
53: Hydrolysis of triacylglycerols
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70
54: Saponification of triacylglycerols
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71
55: Phospholipids
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72
56: Cell membranes
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73
57: Cholesterol and steroids
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74
58: Fat-soluble vitamins
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75
59: Introduction to carbohydrates
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76
60: Monosaccharides
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77
60a: Drawing monosaccharides
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78
61: Drawing cyclic aldoses
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79
62: Drawing cyclic ketoses
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80
62a: Drawing cyclic monosaccharides
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81
63: Reduction and oxidation of monosaccharides WITH ERROR, PLEASE READ DESCRIPTION!!
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82
63a: Reduction and oxidation of monosaccharides
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83
63b: Disaccharides
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84
64: Polysaccharides
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85
65: Blood type
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86
66: Amino acids
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87
67: Structure of nonpolar and neutral amino acids at various pH
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88
68: Structure of acidic amino acids at various pH
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89
69: Structure of basic amino acids at various pH
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90
69b: Amino acids at various pH values
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91
70: Peptides
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92
70a: Drawing peptides
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93
71: Proteins: Primary and secondary structures
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94
72: Proteins: Tertiary and quaternary structures
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95
73: Protein hydrolysis and denaturation
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96
74: Enzymes, cofactors, and inhibitors
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97
75: Nucleotides
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98
76: Nucleic acids
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99
77: The double helix
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100
77a: Writing complimentary strands of DNA
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101
78: An introduction to DNA replication
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102
79: RNA vs. DNA
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103
80: Transcription
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104
81: The genetic code
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105
82: Translation and protein synthesis
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106
81a: How to write a sequence of amino acids from mRNA strand
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107
Lab 1 (Hydrocarbons) Post-lab tutorial
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108
Lab 2 (Analgesics) post-lab tutorial
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109
Lab 3 (Extraction) post-lab tutorial
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110
Lab 4 (Esters) post-lab tutorial
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111
Lab 5 (Soap) post-lab tutorial
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112
Lab 6 (Milk) post-lab assignment
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113
Lab 8 (Enzyme activity) post-lab assignment
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114
ALEKS: Names and symbols of important elements
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115
ALEKS: Writing a chemical formula given a chemical structure
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116
ALEKS: Identifying hydrogen-bonding interactions between molecules
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117
ALEKS: Interpreting the skeletal structure of a neutral organic molecule
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118
ALEKS: Identifying organic functional groups
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119
ALEKS: Naming alkyl side chains
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120
ALEKS: Naming the parent hydrocarbon of branched alkanes
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121
ALEKS: Identifying constitutional isomers
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122
ALEKS: Drawing a skeletal structure from a simple condensed structure
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123
ALEKS: Naming and drawing simple substituted cycloalkanes
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124
ALEKS: Naming and drawing branched alkanes
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125
ALEKS: Drawing the condensed structure of a constitutional isomer
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126
ALEKS: Drawing a skeletal structure from a condensed structure
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127
ALEKS: Naming unbranched alkenes and alkynes
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128
ALEKS: Classifying organic reactions
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129
ALEKS: Interpreting a skeletal structure with aromatic rings
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130
ALEKS: Predicting the reactants or products of alkene hydrogenation
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131
ALEKS: Predicting the reactants or products of alkene hydration
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132
ALEKS: Predicting the products of symmetric alcohol dehydration
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133
ALEKS: Predicting the reactants or products of alcohol oxidation
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134
ALEKS: Drawing the cis or trans isomer of a small alkene
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135
ALEKS: Naming and drawing alcohols
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136
ALEKS: Naming alkenes and alkynes
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137
ALEKS: Identifying chiral centers in a cyclic molecule
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138
ALEKS: Identifying a chiral molecule from its condensed structure
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139
ALEKS: Drawing the mirror image of a simple organic molecule
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140
ALEKS: Identifying the enantiomer of a simple organic molecule
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141
ALEKS: Predicting the reactants or products of esterification
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142
ALEKS: Predicting the reactants or products of alcohol or aldehyde oxidation
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143
ALEKS: Predicting the reactants or products of carbonyl reduction
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144
ALEKS: Naming and drawing ketones
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145
ALEKS: Naming and drawing aldehydes
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146
ALEKS: Identifying and drawing hemiacetals and acetals
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147
ALEKS: Naming and drawing carboxylic acids
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148
ALEKS: Naming and drawing unsubstituted esters
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149
ALEKS: Predicting the reactants or products of hemiacetal and acetal formation
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150
ALEKS: Predicting the reactants or products of acetal hydrolysis
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151
ALEKS: Predicting the reactants or products of ester hydrolysis
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152
ALEKS: Predicting the products of ester saponification
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153
ALEKS: Recognizing organic acids and bases
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154
ALEKS: Identifying primary, secondary, and tertiary amines
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155
ALEKS: Predicting the reactants or products of esterification
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156
ALEKS: Identifying parts of a triacylglycerol
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157
ALEKS: Identifying the parts of a glycerophospholipid
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158
ALEKS: Identifying the parts of a sphingomyelin
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159
ALEKS: Identifying molecules that could be in a cell membrane
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160
ALEKS: Understanding the descriptive vocabulary of monosaccharides
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161
ALEKS: Identifying a given carbon in a cyclic monosaccharide
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162
ALEKS: Naming and drawing the products of aldose oxidation and reduction
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163
ALEKS: Drawing the Haworth projection of an aldose from its Fischer projection
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164
ALEKS: Drawing the Haworth projection of a ketose from its Fischer projection
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165
ALEKS: Identifying the parts of a disaccharide
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166
ALEKS: Understanding the glycosidic links in common polysaccharides
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167
ALEKS: Classifying amino acids
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168
ALEKS: Understanding the general acid-base properties of amino acids
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169
ALEKS: Understanding basic models of competitive and noncompetitive inhibition
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170
ALEKS: Naming an element of a protein secondary structure from a description
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171
ALEKS: Identifying and drawing peptide bonds
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172
ALEKS: Describing peptides with 3-letter codes
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173
ALEKS: Predicting the location in a protein of a residue sequence
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174
ALEKS: Writing complimentary DNA sequences
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175
ALEKS: Numbering the carbons in nucleotides
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176
ALEKS: Recognizing nucleotides
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177
ALEKS: Understanding the structure of nucleic acid strands
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178
ALEKS: Understanding the relationship between DNA and mRNA base sequences
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179
ALEKS: Using the genetic code
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